Table of Contents

101 Eligibility

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§ 102 - Anticipation

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103 - OBVIOUSNESS

AliveCor v. Apple: It is obvious to apply known machine-learning techniques to detect arrhythmia whether the heartbeat data originates from PPG, motion-sensor, or ECG.

The Federal Circuit affirmed PTAB findings that challenged claims were obvious where evidence supported motivation-to-combine and reasonable-understanding findings regarding machine-learning and ECG confirmation limitations.

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Honeywell Int'l v. 3G Licensing: Any need or problem that the patent addresses can supply a reason to make the claimed modification; the patentee's avowed purpose does not control.

The Federal Circuit reversed a Board's determination that claims directed to codeword formatting for error correction is not obvious, finding the Board improperly relied on the motivation of the patent in suit. The Board acknowledged that the only difference between claim 1 and the prior art is that the 1 and 0 in the last row of basis sequences table were switched. The court held that, contrary to KSR, the Board ignored principle that any need or problem known in the field of endeavor at the time of the invention and addressed by the patent can provide a reason for combining the elements in the manner claimed.

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ImmunoGen v. Coke Morgan Stewart: Known dosing methodology to address a known problem in a predictable way is obvious to try

The Federal Circuit affirmed a bench-trial judgment that method claims were obvious where prior art disclosed similar dosing parameters and adjusted ideal body weight (AIBW) dosing was within routine optimization, including where the claimed dose is necessarily met for some patients under a prior-art TBW regimen.

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Janssen Pharma. v. Teva Pharma USA: Presumption of obviousness where ranges overlap

The Federal Circuit held that, in overlapping-range cases, a challenger may establish a presumption of obviousness, i.e., a prima facie case of obviousness, by showing that the claimed values fall within or near prior-art ranges under circumstances where a skilled artisan would have been motivated to optimize and would reasonably expect similar properties. That showing shifts the burden of production, not the burden of persuasion.

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Shockwave Medical v. Cardiovascular Systems: Routine design choice

The Federal Circuit reversed the Board's determination of non-obviousness as to claim 5, saying “The Board [failed] to consider the combined teachings of the prior art led it to improperly discount CSI’s argument in its petition that modifying Uchiyama to place the electrodes outside the lumen would have been a routine design choice. “When there is a design need or market pressure to solve a problem and there are a finite number of identified, predictable solutions, a person of ordinary skill has good reason to pursue the known options within his or her technical grasp.” KSR, 550 U.S. at 421. We explained in Uber Technologies, Inc. v. X One, Inc., 1) that when there are a limited number of well-known design choices in the prior art it would have been obvious to substitute one for the other.

Nonobviousness Secondary-Considerations

Ancora Tech. v. Roku: Nexus of secondary consideration is not negated merely because other patents may also be implicated or because the license arose from settlement

The Federal Circuit affirmed PTAB's prima facie obviousness finding but vacated because objective indicial were mishandles. Specifically, the Board applied an improperly heightened nexus requirement to licenses offered as objective indicia of nonobviousness, requiring reconsideration and reweighing on remand.

Issue/Holding: The nexus standard for patent licenses offered as objective indicia of nonobviousness: For licenses to the challenged patent, the Board may not demand product-style claim-by-claim or feature-parsing nexus showings; licenses are inherently tied to the patented technology, and nexus is not negated merely because other patents may also be implicated or because the license arose from settlement.


Bayer Pharma v. Mylan Pharma: Clinical proof of efficacy does not imply a nexus to the merits of the invention therefor cannot establish nonobviousness

The Federal Circuit held that that Bayer's “unexpected results” theory lacked a nexus because it relied solely on a functionally unrelated limitation (“clinically proven effective”) so secondary considerations did not overcome obviousness.

  • Whether clinical proof of efficacy constitutes unexpected results sufficient to support nonobviousness.: Secondary-consideration evidence must have a nexus to what is claimed and novel; where the asserted “unexpected result” depends solely on a functionally unrelated limitation (clinical proof of efficacy), there is no nexus to the merits of the invention and the evidence cannot establish nonobviousness.


Shockwave Medical v. Cardiovaacular Sys.: Excitement of potential commercial success is “weak” evidence of objective indicia

The Federal Circuit affirmed obviousness, upholding the Board's findings that Shockwave was not entitled to a presumption of nexus with respect to secondary considerations because its objective indicia evidence did not outweigh evidence of obviousness.

  • Presumption of nexus and weighing of secondary considerations in obviousness.: A patentee is entitled to a presumption of nexus only upon showing that the objective evidence is tied to a specific product and that the product embodies the claimed features; the Board may discount conclusory expert assertions and must perform a reasoned collective weighing, which was satisfied here.

Prior Art

ams-OSRAM USA v. Rensas Electronics America: “Proper accessibility” in Texas

The Federal Circuit reversed Judge Mazzant in the Eastern District of Texas on his holding that a trade secret first became accessible when Intersil successfully reverse-engineered the trade secret from TAOS' product. The court held that:

Under Texas law, information that is generally known or readily available by independent investigation is not secret for purposes of trade secrecy. Information cannot be the subject of a trade secret if it is readily ascertainable without engaging in tortious behavior. The practical focus of the inquiry reflects the need to ensure that a tradesecret remedy is tailored to preventing or negating the unfair advantage derived from improper acquisition. A trade secret becomes “properly accessible” where the secret is embodied in a publicly available product: Under Texas trade-secret principles, information is not secret once it is readily ascertainable by proper means, including straightforward reverse engineering after public release; proper accessibility does not depend on when the misappropriator actually succeeded in reverse engineering.

In Re Riggs: The provisional application relied upon for priority must provide written description support for portions of the reference relied upon for the rejection

The Federal Circuit held that a published application's pre-AIA § 102(e) date can reach back to a provisional only for subject matter in the published application that is actually supported in the provisional, and vacated the Board's decision for lacking that analysis.

Lynk Labs v. Samsung Electronics Co.: Pre-AIA 102(e)(1) reference is prior art as of its filing date, even if published after the challenged patent's priority date

The Federal Circuit affirmed the Board's unpatentability determination in an inter-partes review applying pre-AIA §§ 102/103 prior art rules within the AIA IPR framework.

In particular, the Federal Circuit held that, in an IPR, a published U.S. application qualifies as a prior-art printed publication as of its U.S. filing date by virtue of pre-AIA § 102(e)(1), even if published after the challenged patent's priority date. Because a published patent application is a “printed publication” and pre-AIA § 102(e)(1) accords such applications prior-art effect as of their U.S. filing date, § 311(b)'s “prior art consisting of patents or printed publications” includes published applications with § 102(e)(1) filing-date priority even if publication post-dates the challenged patent’s priority date.

Merck Serono v. Hopewell Pharma Ventures: Pre-AIA §  1-2(a)/(3): “by another” includes overlapping inventors

The Federal Circuit clarified the pre-AIA meaning of “by another” or “by others” under §  102(a)/(e) when a reference and the challenged patent have overlapping inventors. Specifically, the court held that, for joint-inventor patents, a reference disclosure is excluded as not “by another” only if the relied-upon disclosure reflects the work of the same inventive entity as the challenged claims. Any mismatch in inventive entity (whether inventors are added or omitted) makes the disclosure “by another” unless the patentee proves teh disclosure was the joint invention of the later inventive entity.

In addition, the court held that the PTAB did not violate the APA by applying identity of inventive entity rule without additional opportunity for evidence or argument. Stated the court: ”Land controls the legal definition of 'by others' or 'by another' in §§ 102(a), (e). Merck thus cannot claim a lack of knowledge of the rule of law based on some arguably contrary language int he MPEP.”

§ 112 Enablement and Written Description

Patent in suit: 8,167,141

Claim 1: A gravity-fed water filter, comprising:

filter media including at least activated carbon and a lead scavenger;

wherein the filter achieves a Filter Rate and Performance (FRAP) factor of about 350 or less according to the following formula: [metric].

Brita LP v. ITC: Single enabled embodiment is insufficient to meet written description or enablement requirements for a broad functional claim

The Federal Circuit affirmed the ITC's holding that Brita's patent for a gravity-fed filter is invalid for lack of written description, lack of enablement, and indefiniteness. The patent lacked written description support for a functionally-defined genus claim that extended beyond the single disclosed species.

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Duke Univ. v. Sandoz: Adequate written description of claimed chemical genus/subgenus

The Federal Circuit reversed the lower District of Colorado decision that claim 30 was non invalid. Specifically, the Federal Circuit held that claim 30 lacked adequate written description support for a claimed chemical genus/subgenus because the written description failed to present either a representative number of species within the claimed scope or disclosure of common structural features with enough precision (i.e., sufficient blaze marks) for a skilled artisan to visualize or recognize the claimed members.

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In re Riggs: Priority date of prior art reference limited by support in the priority document

The Federal Circuit reversed the PTAB's finding of invalidity based on a § 102(e) prior art reference. To predate the critical date, the Board accorded to the reference a priority date based on the filing date of the provisional application, and cited Dynamic Drinkware for the proposition that so long as a single claim is supported by the priority document (i.e., the provisional application) then all of the content of the application is accorded that priority date.

The Federal Circuit vacated PTAB's assertion that a previously filed patent application qualifies as prior art under Dynamic Drinkware. Stated the court: “to claim priority to the provisional filing date, the portion of the application relied on by the examiner as prior art must be supported by the provisional application.”


Sage Products v. Stewart: Enablement when demonstrated by a second reference.

Here, the Federal Circuit held that enablement of an anticipatory reference may be supported by a second references that demonstrates the claimed subject matter was in the public’s possession or could be practiced by skilled artisans using routine/known techniques; considering additional references to assess the state of the art is permissible and does not necessarily constitute impermissible gap-filling.


Seegan v. Daiichi Sankyo Co.: Broad genus disclosure insufficient to support/enable later-claimed subgenus

The Federal Circuit reversed the Eastern District of Texas' denial of Daiichi's JMOL motion for dismissal of the jury verdict based on the claims being unsupported by sufficient written description and non-enabled. Because the patent relied on a priority date of a previously-filed application to predate the sale of Daiichi's cancer drug, Enhertu, the court commented that “one cannot avoid the suspicion that the '039 patent was filed specifically to encompass Enhertu, which is permissible if it was entitled to a filing date antedating any public disclosure of Enhertu.”

The court held:

  • When claims broadly cover any member of a large and unpredictable class and are defined by functional performance, a specification that provides no common quality enabling all functional embodiments and instead requires extensive assay-based, trial-and-error screening does not enable the full scope without undue experimentation under §112(a) (as explained in Amgen v. Sanofi).
  • A disclosure of a very broad genus (millions of potential species) does not satisfy written description for a later-claimed subgenus absent reasonably specific disclosure or “blaze marks” that direct skilled artisans to the particular subgenus; speculative modification paths or “leaps” to the subgenus are insufficient to show possession as of the priority date.
  • Expert testimony that skilled artisans could arrive at a claimed subgenus only by making a “straightforward leap” from disclosed examples confirms, rather than cures, the absence of written description because §112(a) requires disclosure of the specific claimed subject matter, not an invitation to infer or modify toward it.


In re: Xencor, Inc.: Jepson claim preambles are limiting and must be enabled.

The Federal Circuit upheld the Appeals Review Panel's ruling that § 112 requires that the specification provide support for the admitted prior art preamble to a Jepson claim as well as the novel subject matter recited after the transitional phrase (e.g., “wherein the improvement comprises”).

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Mondis Tech. v. LG Electronics: District court reversed on unsupported identifier mapping

The Federal Circuit reversed the District of New Jersey because the amended claim limitation requiring an ID number that identifies at least a type of display unit lacked written-description support in the originally filed specification, which only disclosed one-to-one identification of specific devices and did not reasonably convey possession of type-based identification.


Novartis Pharma. v. Torrent Pharma: Enablement not required as to infringed product

The Federal Circuit reversed the Distr. of Delaware's finding that that the '659 patent was required to describe the full scope of the asserted claims, including the accused complexes sold by Novartis.

Specifically, the Federal Circuit held that § 112 written description requires that the specification reasonably conveys possession of the claimed subject matter; it need not describe unclaimed later-discovered features (such as a complexed form) even if an accused product practicing those features may infringe the properly construed claims.

§ 112 INDEFINITENESS

Akamai Tech. v. MediaPointe: Objective boundaries needed for “optimal” or “best” in claim

Claim 1. A system [. . .] wherein the management center comprising a mapping engine that is configured to map trace routes between the management center, at least one of the nodes, and at least the first client so as to determine one or more optimal routes. . . .“

The Federal Circuit affirmed invalidity where degree terms (“optimal,” “best”) lacked objective boundaries in the intrinsic record, despite reference to trace-route measurements. The court held that terms of degree are indefinite unless the specification/prosecution history supply objective boundaries that allow a skilled artisan to determine scope with reasonable certainty; merely requiring use of trace-route data does not cure indefiniteness where the intrinsic record leaves open-ended which factors apply and how to resolve tradeoffs among metrics that can diverge. A claim’s requirement to use a tool or dataset (here, trace routes) does not provide an objective boundary if it is non-exclusive (other factors may be considered) and does not specify how to choose among multiple potentially conflicting measurement methods or combinations.


Canatext Completion Solutions v. Wellmatics: Antecedent basis error non-fatal

The Federal Circuit reversed an indefiniteness holding based on missing antecedent basis error by concluding the claim contained an obvious error that can be judicially corrected. Because the issue was resolved on intrinsic evidence without fact findings, the court treated the matter as de novo claim interpretation and rejected reliance on expert testimony not supplying extrinsic facts. The court also confirmed that the judicial correction is unavailable if the prosecution history suggests a different interpretation, and found no such prosecution-history indication here.

The court held that it may judicially correct claim language only under a demanding standard: the error must be evident on the face of the patent to a skilled artisan, the correction must not be subject to reasonable debate based on the claims and specification, and the prosecution history must not suggest a different interpretation (and, at least here, the correct is a simple or minor textual change).

Claim Construction

Akamai Technologies v. MediaPointe: “Received by a management center” means the “request” is properly limited to an electronic message, not the act of entering a URL into a browser

The Federal Circuit held that the ordinary meaning of an unconstructed limitation still must be a reasonable meaning in context. Here, it was reasonable for a jury to find that “request . . . received by a management center” is limited to a computer message. Even when a limitation is left to ordinary meaning, the factfinder may adopt only meanings that are reasonable in context; language requiring a “request” to be “received by” a management center reasonably denotes a computer message capable of being received, not a user’s generalized “attempt” to access content.


Alnylam Pharmas. v. Moderna: Claim term limited to express definition despite being qualified by “unless otherwise specified” and dependent claim differentiation argument

The Federal Circuit affirmed the Delaware district court's ruling that the specification's “Definitions” section controls the meaning of the claimed term where it appears unless the patent clearly and explicitly says otherwise. Here, the court rejected the logic that, where a dependent claim is presumed to further narrow the asserted independent claim, the defined term must be more broadly construed because the dependent claim, in this case, can still narrow the independent claim in a different way without contradicting the definition.

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Apple v. Gesture Techn. Partners: Plain meaning does not import implication

The Federal Circuit affirmed the lower court's interpretation of a dependent claim requiring “a light source for illuminating said object” as not requiring that the light source illuminate the object while the camer means obtains an image of the object. The court held that it will not import an unstated temporal or antecedent-basis limitation into a dependent claim.


Bayer Pharma v. Mylan Pharmas.: Functionally unrelated limitations; “product comprising” two ingredients must be a single dosage form or product containing both ingredients

The Federal Circuit held that adding the limitation “clinically proven effective” cannot confer patentability to an otherwise anticipated or obvious treatment method, making inherent anticipation analysis unnecessary. The court distinguished Allergan Sales v. Sandoz 2) stating that the phrase “clinically proven effective” does not further limit the claimed invention since the claims already specify exact dosages to be administered and therefore the additional limitation “clinically proven effective” does not further define the dosages that are administered.

The Federal Circuit also found that the phrase “a first product comprising rivaroxaban and aspirin” requires a single dosage form/product containing both rivaroxaban and aspirin; construing it to cover separate dosage forms would improperly render “a first product comprising” meaningless and is inconsistent with the specification’s distinction between separate dosage forms and a combination dosage form.


Causam Enterprises v. Ecobee Techs: PTAB's refusal to accept patent owner's proposed construction incorporating temporal component

The Federal Circuit affirmed the Board's construction of a key limitation, rejecting an added restriction not supported by the claim language and disfavored because it would exclude disclosed embodimetns. The court held that claim language requiring data to “correspond” to a power reduction does not, without more, impose a temporal restriction on when the data are generated, and constructions that would exclude disclosed embodiments (e.g., estimates or database-derived values measured before or after an event) are disfavored.


In re Xencor: “Treating a patient” in preamble is limiting because another portion of the preamble is referred from the claim body, and the two preamble portions cannot, in this instance, be split into limiting and non-limiting parts

The Federal Circuit agreed with the ARP that “the preamble term 'treating a patient by' is limiting. First, it is important that Xencor does not dispute that the second part of the preamble, 'administering an anti-C5 antibody,' is limiting. The claim language refers back to this section of the preamble—'wherein said anti-C5 antibody with said amino acid substitutions has increased in vivo half-life as compared to said antibody without said substitutions.' At least one portion of the preamble is therefore limiting. Although we may split a preamble into limiting and non-limiting parts, and have done so in cases such as TomTom, Inc. v. Adolph, 3), the preamble here 'cannot be neatly packaged into two separate portions.' Bio-Rad Lab’ys, Inc. v. 10X Genomics Inc., 4). Here, the phrase 'treating a patient' is directly connected with the word 'by' to the phrase 'administering an anti-C5 antibody.' And given our 'disinclination' to 'splic[e]' a preamble into limiting and non-limiting parts, id. at 1371, this lends credence to the argument that the entire preamble should be considered limiting.”


Merck Serono v. Hopewell Pharma Ventures: Claimed dosing of an amount in mg/kg does not require weight-based dosing steps

The Federal Circuit rejected an implied patient-weight determination limitation when a claim recited a dose expressed in mg/kg amounts. The court held that claims reciting a “total dose reached” expressed in mg/kg do not, without an explicit step, require determining patient weight or performing weight-based dosing calculations; a prior-art disclosure (or infringement) can satisfy the limitation based on the administered dose fitting the claimed range regardless of how that dose was determined.


Regeneron Pharmas. v. Mylan Pharmas.: Becton presumption applies to pharmaceutical formulation claim that separately formulation components

The Federal Circuit affirmed a denial of preliminary injunction based on a substantial question of noninfringement because the accused product lacked separately claimed component under the adopted construction, where separately recited “VEGF antagonist” and “buffer” are presumed to be distinct under Becton.

The court held:

  • When a claim recites a composition as comprising separately listed elements, there is a rebuttable presumption (a “clear implication”) that those elements are distinct components; that framework applies to pharmaceutical formulation claims that list “VEGF antagonist” and “buffer” separately.
  • To rebut the presumption of separateness, the patent record must support that a single structure/component can satisfy both limitations; where the claims and specification consistently treat the limitations as separate (including different concentration units and embodiments always using a plus-separate component), the presumption is not overcome.


Rex Medical v. Intuitive Surgical: A “beam [that] comprises an upper portion and a lower portion and a web coupled between the upper portion and the lower portion . . . configured to cause the staple pusher to move a staple” does not imply an I-beam shape

Here, the Federal Circuit held that, absent intrinsic evidence clearly narrowing scope, courts should not import limitations from a depicted embodiment to confine a broader claim term (here, “lower portion”) to a specific I-beam substructure when the claim does not require an I-beam.

Shockwave Medical v. Cardiovascular Systems: “Angioplasty balloon,” in the context of a device for pulverizing hardened vascular plaque, does not require that the balloon press plaque into the vessel wall

The Federal Circuit held that absent clear claim language, specification support, or prosecution disclaimer, “angioplasty balloon” is not limited to balloons that displace plaque into the vessel wall; adding “angioplasty” during prosecution without clear narrowing statements does not create a disclaimer of broader scope.


Sierra Wireless v. Sisvel: “Mutually exclusive” conditional language in claims

Claim 1: A method of performing automatic repeat request (ARQ) in a wireless communication system, the method performed by a receiver and comprising:

[a] detecting whether at least one data block to be received from a transmitter is missed;

[b] starting a timer when the at least one data block is detected as missed;

[c] stopping the timer when the at least one data block is received from the transmitter while the timer is running, in order to prevent a triggering of a status report before the timer expires; and

[d] transmitting the status report to the transmitter after the timer expires, wherein the status report comprises a positive acknowledgement indicating receipt of at least one received data block.

The Federal Circuit rejected the Board's reasoning that limitations 1[c] and 1[d] are mutually exclusive and “cannot both occur i response to the same set of stimuli” because the timer either stops . . . or expires.” The court said “that conclusion does not follow from the premise describing the claim language. [. . .] Here, we reject the Board's conclusion because the plain and unambiguous language of claim 1 requires that a method, to come within the claim, must perform both limitations 1[c] and 1[d] where their preconditions apply.” This opinion effectively supersedes the PTAB's precedential ruling in Ex Parte Schulhauser.

The opinion also reinforces procedural rigor at the PTAB: expert testimony on anticipation and obviousness must come from at least a person of ordinary skill in the art as defined by the Board. Because the Board credited testimony from a declarant who lacked the required qualifications without making a specific finding that his experience sufficed, the Federal Circuit vacated the decision for abuse of discretion.

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Sigray v. Carl Zeiss X-Ray Microscopy: Magnification of 1X - 10X includes 1

The court held claims anticipated due to inherent disclosure of prior art, finding that the Board improperly and implicitly construed the claimed numeric magnification range (between 1 and 10) to exclude small magnification (that was inherent to the prior art due to non-parallel rays) and held that construction erroneous under the claim's plain meaning. A tribunal engages in claim construction when its reasoning effectively narrows a claim term’s scope (e.g., by requiring divergence “enough” to produce a certain level of magnification); absent intrinsic evidence to the contrary, a numeric range’s plain meaning controls and includes even very small values within the endpoints.

Claim Construction - Reliance on Intrinsic Evidence

Aortic Innovations v. Edwards Lifesciences: Implied narrowing of term by interchangeable use in specification

The Federal Circuit affirmed construing “outer frame: as a “self-expanding frame” based on clear implied lexicography via consistent interchangeable use in the specification. Because the accused device's frame expanded only with the assistance of a balloon, it did not read on the claimed “outer frame.”

Holdings:

  • A patent’s clear and consistent interchangeable use of a claim term with a narrower term in the specification can constitute implied lexicography that equates the terms, supporting a construction that imports that narrower meaning into the claim.
  • Where the specification repeatedly characterizes the claimed “outer frame” in transcatheter-valve embodiments as a self-expanding frame and the claim’s “inner frame” (undisputedly) is balloon-expandable, construing “outer frame” as “self-expanding frame” is proper.


FMC v. Sharda USA: Importing a narrowing definition dropped from provisional application is improper

The Federal Circuit reversed the lower court's claim construction that relied on a narrowed interpretation based on a discussion in the provisional application but not in the asserted patent. The court held that when the patentee materially deletes limiting terminology (here, stability-related disclosures) between a provisional application and the issued patent’s specification, those deleted disclosures cannot be used to re-impose the deleted limitation in claim construction; the claim term should receive its plain and ordinary meaning absent other intrinsic support. Although similar claim terms in related patents are often construed consistently, that presumption yields where the patentee materially altered the specification in certain family members in a way that would direct a skilled artisan to understand a different intended meaning.

The court also rejected an attempt by FMC to narrow the claim scope based on a use in the pramble. Preamble language that merely states a purpose or intended use generally is not limiting. Moreover, differences in preamble wording across claims do not make the preamble limiting absent a basis to treat the preamble as claim scope-defining.


HD Silicon Solutions v. Microchip Tech.: Intrinsic evidence controls interpretation of “comprising tungsten” as “elemental tungsten” and not compounds thereof

The Federal Court construed “comprising tungsten” to require elemental tungsten and held the Board's broader construction was incorrect, emphasizing intrinsic evidence over extrinsic evidence. Where the intrinsic record uses explicit compound nomenclature when compounds are intended (e.g., “titanium nitride”) and otherwise discusses a material only as the element with element-specific properties, “comprising [element]” is properly construed to require the elemental form (allowing incidental impurities) rather than encompassing compounds of that element. Extrinsic evidence (including other patents/publications) may assist understanding but cannot be used to vary or expand a claim meaning that is indicated by the patent’s claims/specification/prosecution history.


Iqris Techs. v. Point Blank Enterprises: Discussion of prior art is not clear and unequivocal disavowal

The Federal Circuit held that the district court improperly imported limitations into the term “pull cord,” rejecting a construction requiring direct pulling by a user and excluding cords with handles. The court held that, absent claim language or clear intrinsic evidence of lexicography/disavowal, a court may not limit “pull cord” to cords directly pulled by a user merely because the specification’s preferred embodiments depict direct pulling or use different labels for other cords.


Lynk Labs v. Samsung Electronics Co.: Intrinsic evidence shows “match” not limited to numerical equivalence

The Federal Circuit construed the claim term “matches” to mean “equal to or less than,” rather than strict equivalence, because the intrinsic evidence consistently describes “matching” in functional, tolerance-based terms rather than exact numerical identity. Reading the claim language in light of the specification as a whole, the court explained that the invention is concerned with avoiding over-driving LEDs, which is satisfied when the rectified input voltage does not exceed the aggregate forward voltage of the LEDs. Nothing in the intrinsic record limits “matches” to exact equality, and multiple passages expressly contemplate a “less than or equal to” relationship, making a broader construction not only reasonable but required.

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Claim Construction - Prosecution disclaimer

Azurity Pharmas v. Alkem Labs.: Adding “consisting of” to avoid prior art is a clear and unmistakable disclaimer

The Federal Circuit held that Azurity clearly and unmistakably surrendered claim scope covering any presence of propylene glycol by inserting “consisting of” the list of ingredients to avoid prior art wherein propylene glycol was used as a stabilizer, even though th list of ingredients included a flavoring agent. Because the accused device included a flavoring agent containing propylene glycol it was non-infringing.

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Barrette Outdoor Living v. Fortress Iron: criticism in spec of prior art feature does not justify construing claims as avoiding that feature

The Federal Circuit affirmed noninfringement based broadly construing “boss” not necessarily fastener-less, despite the patent's discussion of multiple advantages of fastener-less bosses. The court held that a patent's discussion of multiple advantages does not justify importing one advantage-related feature into claims absent absent clear and unmistakable disclaimer; here, criticism of fastener-based prior art did not clearly limit “boss” to fastener-less structures.


Eye Therapies v. Slayback Pharma: “Consisting essentially of” narrowed by prosecution disclaimer

The Federal Circuit relied on prosecution history statements accompanying an amendment define the scope of “consisting essentially of,” treating explanatory remarks and definitional “i.e.” usage as limiting. The court held that although “consisting essentially of” is typically semi-open, the intrinsic record can assign it an atypically restrictive meaning; here, the prosecution history establishes that the phrase excludes use of active ingredients other than brimonidine in the claimed methods. When the applicant uses “i.e.” to equate a claim phrase with a particular meaning in prosecution arguments, that usage is strongly definitional and supports construing the claim phrase consistently with the stated definition. Where claims were narrowed during prosecution, claims need not cover every described embodiment.


Focus Products Group Internat'l v. Kartri Sales Co.: Election of species without objection is disclaimer of non-elected species

The Federal Circuit reversed the District Court for the Southern District of NY based on corrected claim scope for a shower curtain “ring.” The court held that prosecution history including restriction and an election to withdraw nonelected species, and prosecution of a divisional application excluding the elected species can constitute clear and unmistakable disclaimer of the claim scope. Here, because the properly construed claims exclude a feature present in the accused product (i.e., rings with flat upper edges) summary judgment of infringement cannot stand and must be reversed as to the party preserving the noninfringement issue.


Maquet Cardiovascular v. Abiomed: Related applicant's prosecution history is relevant only when the earlier prosecution addresses a limitation in common with the claim term being construed

The Federal reversed and remanded to the district court's claim construction claims with added negative limitations. The court held that prosecution disclaimer from a related patent's prosecution is relevant only when the earlier prosecution addresses a limitation in common with the claim term being construed; material differences in claim language (e.g., claiming an “entire elongate lumen distal to” a component versus a “guide mechanism comprising a lumen”) defeat reliance on that history to import a negative limitation.


Restem v. Jadi Cell: Applicant's acquiescence to Examiner's repeated characterization constituted disavowal

The Federal Circuit held that clear examiner statements characterizing the allowed claim scope, coupled with applicant acquiescence during prosecution, can narrow claim scope (here, to a “cell population”), and that narrowed understanding may control over broader specification disclosures/definitions.

112(f) Means Plus Function

Fintiv v. PayPal Holdings: “handler” is a nonce term

The Federal Circuit held that the district court correctly analogized “handler” with the nonce term, “module” which was previously determined to be a generic description of software or hardware that performs a specified function. The prefix “payment” (for “payment handler”) did not impart structure and merely describes the function of the handler: to perform payment functions. The Federal Circuit further agreed with the district court that the specifications of the asserted patents do not disclose any algorithm to perform the recited function, and held the payment-handler terms indefinite.

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Optis Cellular Technology v. Apple: District court's reasoning that “selecting unit” does not invoke § 112 ¶ 6 failed to explain how the selecting unit operates

The Federal Circuit held that “selecting unit” invoked § 112 ¶ 6 and remanded for the corresponding structure and indefiniteness analysis. More specifically, the court found that a “unit” term modified only by functional language (e.g., “selecting”/“configured to randomly select”) is a nonce term that fails to connote sufficiently definite structure and therefore invokes § 112 ¶ 6; remand is appropriate for the district court to determine whether the specification discloses adequate corresponding structure (and resulting definiteness).


Steuben Foods v. Shibuya Hoppmann: District court's JMOL reversed; infringement found under § 112 ¶ 6 “equivalents” standard

The Federal Circuit reversed the district court's JMOL of noninfringement for a § 112 ¶ 6 “means for filling” limitation where substantial evidence supported that accused structures were equivalent in the context of the claimed function. For a § 112 ¶ 6 limitation, structural differences must be assessed in the context of the claimed function and the overall corresponding structure; substantial evidence can support equivalence where accused components perform the identical function in substantially the same way with substantially the same result, even if component-level details differ.

IPR Institution

IGT v. Zynga: Decision not to apply interference estoppel as a bar to institution is nonappealable

The Federal Circuit held that the PTO's decision not to apply interference estoppel as a bar to institution is a nonappealable institution determination under 35 U.S.C. § 314(d), with no Cuozzo “shenanigans” exception on these facts. The court also rejected a procedural challenge that the Board relied on a new, unargued unpatentability theory, finding adequate notice and opportunity to respond under IPR due-process/APA principles.

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AIA_ESTOPEL_TIME_BARS_JURISDICTION

- Appl 23-1475.pdf

- In re Gesture 25-1075.pdf

- Ingenico 23-1367.pdf

AIA_EVIDENCE_BURDENS_STANDARDS

- Alivecor 23-1512.pdf

- Amp Plus 23-1997.pdf

- Apple 23-1501.pdf

- Centripetal 23-2027.pdf

- Dolby 23-2110.pdf

- Global Health 23-2009.pdf

- Honeywell 23-1354.pdf

- IBM 24-1170.pdf

- In re PT Medisafe Tech. 23-1573.pdf [NEEDS_REVIEW]

- Kroy IP 23-1359.pdf

- Lashify 23-1245.pdf

- Lynk Labs 23-2346.pdf

- Merck 25-1210.pdf

- Shockwave Medical 23-1864.pdf

AIA_MERITS_102_103_112

- Alivecor 23-1512.pdf

- Amp Plus 23-1997.pdf

- Ancora 23-1674.pdf

- Appl 23-1475.pdf

- Apple 23-1501.pdf

- Bayer Pharma 23-2434.pdf

- Causam 24-1958.pdf

- Global Health 23-2009.pdf

- HD Silicon 23-1397.pdf

- Honeywell 23-1354.pdf

- IBM 24-1170.pdf

- IGT 23-2262.pdf

- Kroy IP 23-1359.pdf

- Lynk Labs 23-2346.pdf

- Qualcomm 23-1208.pdf

- Restem 23-2054.pdf

- Shockwave Medical 23-1864.pdf

AIA_PROCEDURE_DUE_PROCESS_APA

- Alivecor 23-1512.pdf

- Amp Plus 23-1997.pdf

- Appl 23-1475.pdf

- CQV 23-1027.pdf

- Causam 24-1958.pdf

- Centripetal 23-2027.pdf

- Honeywell 23-1354.pdf

- IBM 24-1170.pdf

- IGT 23-2262.pdf

- In re Bayou Grand Coffee 24-1118.pdf [NEEDS_REVIEW]

- In re Riggs 22-1945.pdf

- Merck 25-1210.pdf

- Odyssey Logistics 23-2077.pdf

- Qualcomm 23-1208.pdf

- Sage Products 23-1603.pdf

- Shockwave Medical 23-1864.pdf

DIRECT_INFRINGEMENT

- Adnexus 24-1551.pdf

  • Sufficiency of pleading direct infringement of a specific limitation where the complaint incorporates claim charts and preliminary infringement contentions.: A patent complaint plausibly states direct infringement when it includes factual allegations (including in attached, incorporated claim charts/analyses) that, taken as true and with reasonable inferences drawn for the patentee, articulate why the accused product meets the challenged claim limitation; element-by-element pleading is not required, but factual content must support plausibility.

- Akamai 24-1571.pdf

  • Summary judgment of noninfringement where accused “management center” receives only DNS queries that do not identify requested media content.: No triable infringement issue exists where undisputed evidence shows the accused component receives only communications that do not satisfy the claim-required “request for media content” element; a noninfringement judgment may be affirmed even assuming the patentee’s expert testimony if that testimony cannot bridge the element-to-evidence gap.

- Azurity Pharma 23-1977.pdf

  • Infringement in a Hatch–Waxman case where the ANDA product contains an ingredient disclaimed from closed “consisting of” claims.: When the ANDA describes a product containing an ingredient excluded by disclaimer and not permitted by a closed “consisting of” claim transition, traditional infringement principles require a finding of noninfringement; where the ANDA directly addresses the infringement issue, it controls the comparison.

- Egenera 23-1428.pdf

  • Summary judgment noninfringement where CPUs did not “emulate Ethernet functionality.”: Where claims require that the “plurality of computer processors” include logic that “emulate[s] Ethernet functionality,” evidence that processors merely use or communicate over Ethernet (while separate components perform the emulation) cannot create a genuine dispute of infringement under the existing, unchallenged claim scope.
  • General verdict rule for multiple alternative noninfringement theories.: A general jury verdict of noninfringement must be upheld if substantial evidence supports any one of the accused infringer’s alternative factual theories submitted to the jury; the appellant must show lack of substantial evidence as to all alternatives to obtain reversal.
  • No improper “intent” requirement from references to “programmed for the claimed purpose.”: A court does not add a scienter/intent element by describing whether an accused system’s components are programmed to perform the claimed functionality; such language can permissibly refer to the functional limitations recited in the claims.

- Finesse Wireless 24-1039.pdf

  • Whether substantial evidence supported the jury’s finding that the accused radios met the ’134 patent limitation requiring sampling a passband that includes both “signals of interest” and “interference generating signals.”: When the patentee’s infringement proof depends on expert testimony that is internally inconsistent and never clearly maps the accused features to the claim limitation, the verdict lacks substantial evidence and JMOL of noninfringement is warranted.
  • Whether substantial evidence supported the jury’s finding that the accused radios performed the seven specific third-order multiplications required by the ’775 patent claims.: Where the claims require performance of a specific set/number of operations, identifying only fewer distinct operations in the accused product—without evidence they correspond to or implement the required set—cannot support an infringement verdict; appellate counsel’s post hoc mapping cannot supply missing trial proof.

- Fraunhofer-Gesellshaft 23-2267.pdf [NEEDS_REVIEW]

  • (no holding tagged to this category)

- Jiaxing Super 23-1715.pdf

  • Whether the jury’s infringement verdict for the ’140 patent was supported and consistent with the no-anticipation verdict.: A finding of no anticipation does not preclude a finding of infringement where evidence supports that the accused product meets the claim limitation at issue while the prior-art reference does not; substantial-evidence review sustains the jury’s infringement verdict when supported by credited expert testimony.

- Lab. Corp. 23-2350.pdf

  • Whether an adaptor-binding primer can satisfy the ’597 patent’s construed “target-specific primer” limitation for literal infringement.: Under a construction requiring that the target-specific primer anneal to and mediate amplification of the target nucleic acid and not anneal to or mediate amplification of non-target sequences, a primer that anneals to a universal adaptor/common sequence present on all molecules does not meet the limitation, even if the adaptor is ligated onto a molecule that also contains a target region.
  • Whether an accused primer can meet a limitation by working “in concert” with a different primer not recited as performing the limitation’s required function.: Where the claim construction and plain claim language require the recited primer itself to perform the specified targeting/non-target-exclusion functions, infringement cannot be shown by combining the accused primer with another primer’s targeting activity to collectively satisfy the limitation.

- Maquet Cardovascular 23-2045.pdf

  • Whether the Federal Circuit should decide infringement in the first instance following a stipulated judgment predicated on claim construction: Where the parties stipulated to noninfringement based on claim construction and infringement was not litigated below, the Federal Circuit will not resolve infringement in the first instance absent a record eliminating genuine issues of material fact and entitling a party to judgment as a matter of law.

- Mitek Systems 23-1687.pdf

  • Direct-infringement-based DJ standing where the patentee never accused the supplier’s product of meeting all claim limitations.: A supplier cannot establish a reasonable potential for a direct infringement suit when undisputed record evidence shows the supplier’s product (as provided) does not and cannot satisfy all claim limitations (including limitations performed by end users or requiring hardware components the supplier does not provide), and the patentee has not accused the supplier’s product alone of meeting every limitation.

- Regeneron Pharma 24-2351.pdf

  • Preliminary-injunction likelihood of success where accused product omits a separately required claim component under the proper construction.: Under the adopted construction requiring distinct “VEGF antagonist” and “buffer” components, a product lacking a separate buffer raises at least a substantial question of noninfringement, defeating the patentee’s showing of likely success on the merits and supporting denial of a preliminary injunction.

- Rex Med. 24-1072.pdf

  • Sufficiency of evidence for a “configured to cause” limitation where an intermediate component is present: Substantial evidence can support infringement of a “configured to cause” limitation where the claimed component is designed/arranged to cause the required result through an intermediate structure (and intent of the designers is irrelevant to direct infringement), especially in an open “comprising” claim that does not exclude additional elements.

- Steuben Foods 23-1790.pdf

  • Whether JMOL of noninfringement based on the reverse doctrine of equivalents (RDOE) can stand where the patentee presented expert rebuttal testimony.: Even assuming RDOE remains available, JMOL is improper where the record contains substantial evidence—such as credited expert rebuttal—supporting the jury’s rejection of the accused infringer’s RDOE theory; the court may not discard rebuttal testimony as a matter of law where it provides an evidentiary basis for the verdict.

- Top Brand 24-2191.pdf

  • Design patent infringement under the ordinary-observer test when key similarities fall within disclaimed subject matter.: When the accused design’s asserted similarities to the patented design lie in features the patentee surrendered during prosecution, those features cannot support an ordinary-observer finding of substantial similarity; if no non-disclaimed similarities support infringement, JMOL of noninfringement is required.

- Trudell Medical 23-1777.pdf

  • Entitlement to JMOL of infringement where defendant’s primary noninfringement expert testimony should have been excluded.: Even if the defendant’s noninfringement expert testimony is excluded, JMOL for the patentee is not required where the jury could reasonably disbelieve the patentee’s evidence and find the patentee failed to carry its affirmative burden of proving infringement.

- Wuhan Healthgen 23-1389.pdf

  • Whether the Commission’s infringement finding could be supported by SEC-HPLC aggregation data not taken precisely at the moment of importation.: In a § 337 infringement determination, the Commission may rely on reliable test data and record evidence to find the accused imported products meet a quantitative claim limitation, and the finding is sustained on appeal where substantial evidence supports that the tested characteristic would not rise above the claimed threshold during ordinary storage and shipment prior to importation.

DOCTRINE_OF_EQUIVALENTS

- Adnexus 24-1551.pdf

  • Whether to reach a district court’s doctrine-of-equivalents/prosecution-history preclusion dismissal after vacating the literal infringement dismissal.: Where the predicate dismissal of the direct infringement claim is vacated, an appellate court may decline to address an alternative doctrine-of-equivalents/prosecution-history preclusion ruling tied to the same limitation and allow further proceedings on remand.

- Colibri Heart Valve 23-2153.pdf

  • Effect of un-rebutted prosecution history estoppel on a doctrine-of-equivalents infringement theory.: Where the Festo presumption applies and the patentee does not invoke or prove an exception (or otherwise justify a narrower surrender), prosecution history estoppel bars the doctrine of equivalents for the surrendered subject matter and can require JMOL of noninfringement when DOE is the only infringement theory.

- Iqris 23-2062.pdf

  • Scope of appellate decision regarding infringement under the corrected construction.: On vacatur based on corrected claim construction, the appellate court may remand for the district court to apply the correct construction in the first instance, including for doctrine-of-equivalents issues, without deciding whether summary judgment is ultimately appropriate.

- Lab. Corp. 23-2350.pdf

  • Sufficiency of evidence for doctrine-of-equivalents infringement of the ’810 patent’s “second target-specific primer.”: A DOE verdict requires limitation-specific, particularized testimony and linking argument showing the accused element has substantially the same function, way, and result as the claimed limitation; where the accused primer binds a common tail/adaptor sequence and does not provide target specificity/enrichment, the evidence is insufficient as a matter of law under function-way-result.

- Smartrend 24-1616.pdf

  • Whether the evidence supported doctrine-of-equivalents infringement of the ’491 patent’s “frame” limitation.: Under the function-way-result test, equivalence must be shown element-by-element and the claimed element’s “function” may be established—sometimes dispositively—by the patent’s written description; where undisputed evidence shows the accused integrated structure cannot perform specification-established functions of the claimed separate element, JMOL of no equivalents infringement is required.

- Steuben Foods 23-1790.pdf

  • Doctrine of equivalents for “intermittently added” limitation construed as “added in a non-continuous manner.”: Where a claim limitation is construed to require non-continuous addition, treating a concededly continuous addition as equivalent would vitiate the limitation; under such a construction, no reasonable juror can find continuous operation equivalent to intermittent operation.

- Wonderland Switzerland 23-2043.pdf

  • Whether DOE can satisfy a claim limitation requiring the seat back to have a “locking mechanism for selectively detachably connecting” when the accused product places the selective-detachability mechanism on a different component.: DOE cannot be used to treat a different claim element as satisfying a limitation; equivalence is evaluated element-by-element, and where the accused seat back lacks any structure for selective detachability required by the seat-back limitation, infringement under DOE fails as a matter of law.

APPELLATE_JURISDICTION_FINALITY

- Acorda Therapeutics 23-2374.pdf

- Amp Plus 23-1997.pdf

- Aortic Innovations 24-1145.pdf

- Broad Institute 22-1653.pdf

- Casam 23-1769.pdf

- Dolby 23-2110.pdf

- Ecofactor 23-1101.pdf

- IQE 24-1124.pdf [NEEDS_REVIEW]

- In re Gesture 25-1075.pdf

- Incyte Pharma 23-1300.pdf

- Maquet Cardovascular 23-2045.pdf

- Micron Tech. 23-2007.pdf

- Odyssey Logistics 23-2077.pdf

- Qualcomm 23-1208.pdf

- Realtek 23-1187.pdf

- USAA 23-1639.pdf

ASSIGNMENT_OWNERSHIP_CHAIN_OF_TITLE

- Casam 23-1769.pdf

ATTORNEYS_FEES_OCTANE

- AMS-Osram 22-2185.pdf

- Escapex IP 24-1201.pdf

- Focus Products 23-1446.pdf

- Future Link 23-1056.pdf

BIOSIMILARS_HATCH_WAXMAN

- Azurity Pharma 23-1977.pdf

- Janssen Pharma 25-1228.pdf

- Jazz Pharma 24-2274.pdf

- Merck Sharp & Dohme 23-2254.pdf [NEEDS_REVIEW]

DAMAGES_APPORTIONMENT_ENTIRE_MARKET_VALUE

- Rex Med. 24-1072.pdf

DAMAGES_LOST_PROFITS

- Wash World 23-1841.pdf

DAMAGES_REASONABLE_ROYALTY

- Ecofactor 23-1101.pdf

- Finesse Wireless 24-1039.pdf

- Jiaxing Super 23-1715.pdf

- Rex Med. 24-1072.pdf

- Wonderland Switzerland 23-2043.pdf

ENHANCED_DAMAGES_WILLFULNESS

- Focus Products 23-1446.pdf

- Wonderland Switzerland 23-2043.pdf

DESIGN_PATENTS

- Lashify 23-1245.pdf

- Smartrend 24-1616.pdf

- Top Brand 24-2191.pdf

DOUBLE_PATENTING

- Immunogen 23-1762.pdf

- Regeneron 24-1965.pdf

EXHAUSTION_AND_IMPLIED_LICENSE

- Fraunhofer-Gesellshaft 23-2267.pdf [NEEDS_REVIEW]

INDIRECT_INFRINGEMENT

- Mitek Systems 23-1687.pdf

INJUNCTIONS_EBAY

- Jazz Pharma 24-2274.pdf

- Regeneron 24-1965.pdf

- Smartrend 24-1616.pdf

- Wonderland Switzerland 23-2043.pdf

INVENTORSHIP_CORRECTION

- Bearbox 23-1922.pdf [NEEDS_REVIEW]

- Coda Development 23-1880.pdf

- Global Health 23-2009.pdf

ITC_SECTION_337

- Brita 24-1098.pdf

- Casam 23-1769.pdf

- Lashify 23-1245.pdf

- Realtek 23-1187.pdf

- US Synthetic 23-1217.pdf

- Wuhan Healthgen 23-1389.pdf

- Ecofactor 23-1101.pdf

- Game Plan 24-1407.pdf

- IQE 24-1124.pdf [NEEDS_REVIEW]

- Agilent 23-2186.pdf [NEEDS_REVIEW]

- Apex Bank 23-2143.pdf [NEEDS_REVIEW]

- Bearbox 23-1922.pdf [NEEDS_REVIEW]

Trademarks

- Bullshine Distillery 23-1682.pdf [NEEDS_REVIEW]

- Ceramtec 23-1502.pdf [NEEDS_REVIEW]

- Dollar Financial Group 23-1375.pdf [NEEDS_REVIEW]

- Fraunhofer-Gesellshaft 23-2267.pdf [NEEDS_REVIEW]

- Heritage Alliance 24-1155.pdf [NEEDS_REVIEW]

- In re Bayou Grand Coffee 24-1118.pdf [NEEDS_REVIEW]

- In re Brunetti 23-1539.pdf [NEEDS_REVIEW]

- In re Foster 23-1527.pdf [NEEDS_REVIEW]

- In re PT Medisafe Tech. 23-1573.pdf [NEEDS_REVIEW]

- In re Vetements Group 23-2050.pdf [NEEDS_REVIEW]

- Sunkist Growers 24-1212.pdf [NEEDS_REVIEW]

- Ceramtec 23-1502.pdf [NEEDS_REVIEW]

?

- IQE 24-1124.pdf [NEEDS_REVIEW]

- Merck Sharp & Dohme 23-2254.pdf [NEEDS_REVIEW]

Patent Term

- In re Forest 23-1178.pdf [NEEDS_REVIEW]

PRECLUSION_RES_JUDICATA_COLLATERAL_ESTOPPEL

- In re Riggs 22-1945.pdf

- Inland Diamond 24-1106.pdf

- AMS-Osram 22-2185.pdf

- Kroy IP 23-1359.pdf

- Wash World 23-1841.pdf

Claims to Priority

- Dollar Financial Group 23-1375.pdf [NEEDS_REVIEW]

IPR Procedure

- In re Gesture 25-1075.pdf

- Centripetal 23-2027.pdf

In an obviousness analysis, the Board must consider all properly presented evidence of secondary considerations (including copying) and assign it whatever weight the evidence warrants; it is reversible error to omit discussion of such evidence on the ground that the Board is not positioned to evaluate the broader litigation record.

Jurisdiction

- Mitek Systems 23-1687.pdf

Damages

PREJUDGMENT_INTEREST_POSTJUDGMENT_INTEREST

- AMS-Osram 22-2185.pdf

PROCEDURAL_CIVIL_RULES

- Acorda Therapeutics 23-2374.pdf

- Adnexus 24-1551.pdf

- Akamai 24-1571.pdf

- Alivecor 23-1512.pdf

- Ancora 23-1674.pdf

- Aortic Innovations 24-1145.pdf

- Appl 23-1475.pdf

- Azurity Pharma 23-1977.pdf

- Bearbox 23-1922.pdf [NEEDS_REVIEW]

- Coda Development 23-1880.pdf

- Colibri Heart Valve 23-2153.pdf

- Dollar Financial Group 23-1375.pdf [NEEDS_REVIEW]

- Ecofactor 23-1101.pdf

- Egenera 23-1428.pdf

- Escapex IP 24-1201.pdf

- Fraunhofer-Gesellshaft 23-2267.pdf [NEEDS_REVIEW]

- Future Link 23-1056.pdf

- Game Plan 24-1407.pdf

- IQE 24-1124.pdf [NEEDS_REVIEW]

- Incyte Pharma 23-1300.pdf

- Ingenico 23-1367.pdf

- Jazz Pharma 24-2274.pdf

- Kroy IP 23-1359.pdf

- Magema Tech. 24-1342.pdf

- Micron Tech. 23-2007.pdf

- Mitek Systems 23-1687.pdf

- Odyssey Logistics 23-2077.pdf

- Optis Cellular 22-1925.pdf

- Powerblock 24-1177.pdf

- Recentive 23-2437.pdf

- Regeneron Pharma 24-2351.pdf

- Steuben Foods 23-1790.pdf

- Top Brand 24-2191.pdf

- Trudell Medical 23-1777.pdf

- US Inventor 24-1396.pdf

- US Synthetic 23-1217.pdf

- Wash World 23-1841.pdf

PROSECUTION_HISTORY_DISCLAIMER_OR_ESTOPPEL

- Finesse Wireless 24-1039.pdf

- Focus Products 23-1446.pdf

- Iqris 23-2062.pdf

- Magema Tech. 24-1342.pdf

- Maquet Cardovascular 23-2045.pdf

- Mondis 23-2117.pdf

- Restem 23-2054.pdf

- Top Brand 24-2191.pdf

REISSUE_REEXAM

- In re Kostik 23-1437.pdf

- Merck Sharp & Dohme 23-2254.pdf [NEEDS_REVIEW]

REMAND_INSTRUCTIONS_AND_SCOPE

- Global Health 23-2009.pdf

- In re Brunetti 23-1539.pdf [NEEDS_REVIEW]

- Sigray 23-2211.pdf

- Smartrend 24-1616.pdf

- Trudell Medical 23-1777.pdf

REMEDIES_CONTRIBUTORY_ISSUES

- AMS-Osram 22-2185.pdf

- Jazz Pharma 24-2274.pdf

- Wash World 23-1841.pdf

SANCTIONS

- Escapex IP 24-1201.pdf

- Future Link 23-1056.pdf

STANDARD_OF_REVIEW_AND_EVIDENTIARY_RULINGS

- Adnexus 24-1551.pdf

- Akamai 24-1571.pdf

- Alivecor 23-1512.pdf

- Alnylam Pharma 23-2357.pdf

- Ancora 23-1674.pdf

- Apex Bank 23-2143.pdf [NEEDS_REVIEW]

- Apple 23-1501.pdf

- Barrette Outdoor Living 24-1231.pdf

- Bearbox 23-1922.pdf [NEEDS_REVIEW]

- Broad Institute 22-1653.pdf

- Bullshine Distillery 23-1682.pdf [NEEDS_REVIEW]

- CQV 23-1027.pdf

- Canatex Completion 24-1466.pdf

- Ceramtec 23-1502.pdf [NEEDS_REVIEW]

- Coda Development 23-1880.pdf

- Colibri Heart Valve 23-2153.pdf

- Dollar Financial Group 23-1375.pdf [NEEDS_REVIEW]

- Duke Univ. 24-1078.pdf

- Ecofactor 23-1101.pdf

- Egenera 23-1428.pdf

- Escapex IP 24-1201.pdf

- Eye Therapies 23-2173.pdf

- FMC 24-2335.pdf

- Finesse Wireless 24-1039.pdf

- Fintiv 23-2312.pdf

- Focus Products 23-1446.pdf

- Fraunhofer-Gesellshaft 23-2267.pdf [NEEDS_REVIEW]

- Future Link 23-1056.pdf

- Game Plan 24-1407.pdf

- Global Health 23-2009.pdf

- HD Silicon 23-1397.pdf

- Heritage Alliance 24-1155.pdf [NEEDS_REVIEW]

- Honeywell 23-1354.pdf

- IGT 23-2262.pdf

- Immunogen 23-1762.pdf

- In re Bayou Grand Coffee 24-1118.pdf [NEEDS_REVIEW]

- In re Brunetti 23-1539.pdf [NEEDS_REVIEW]

- In re Foster 23-1527.pdf [NEEDS_REVIEW]

- In re Kostik 23-1437.pdf

- In re PT Medisafe Tech. 23-1573.pdf [NEEDS_REVIEW]

- In re Vetements Group 23-2050.pdf [NEEDS_REVIEW]

- In re Xencor 24-1870.pdf

- Incyte Pharma 23-1300.pdf

- Ingenico 23-1367.pdf

- Inland Diamond 24-1106.pdf

- Iqris 23-2062.pdf

- Janssen Pharma 25-1228.pdf

- Jiaxing Super 23-1715.pdf

- Kroy IP 23-1359.pdf

- Lab. Corp. 23-2350.pdf

- Magema Tech. 24-1342.pdf

- Mondis 23-2117.pdf

- Odyssey Logistics 23-2077.pdf

- Optics Cellular 22-1925.pdf

- Powerblock 24-1177.pdf

- Regeneron 24-1965.pdf

- Regeneron Pharma 24-2351.pdf

- Rex Med. 24-1072.pdf

- Sage Products 23-1603.pdf

- Sierra Wireless 23-1059.pdf

- Smartrend 24-1616.pdf

- Steuben Foods 23-1790.pdf

- Sunkist Growers 24-1212.pdf [NEEDS_REVIEW]

- Top Brand 24-2191.pdf

- Trudell Medical 23-1777.pdf

- US Inventor 24-1396.pdf

- US Synthetic 23-1217.pdf

- USAA 23-1639.pdf

- Wonderland Switzerland 23-2043.pdf

- Wuhan Healthgen 23-1389.pdf

STANDING_AND_CASE_OR_CONTROVERSY

- Aortic Innovations 24-1145.pdf

- Apple 23-1501.pdf

- CQV 23-1027.pdf

- Casam 23-1769.pdf

- Causam 24-1958.pdf

- Curtin 23-2140.pdf

- Dolby 23-2110.pdf

- Focus Products 23-1446.pdf

- Game Plan 24-1407.pdf

- In re Brunetti 23-1539.pdf [NEEDS_REVIEW]

- In re Forest 23-1178.pdf [NEEDS_REVIEW]

- In re Gesture 25-1075.pdf

- Incyte Pharma 23-1300.pdf

- Mitek Systems 23-1687.pdf

- Odyssey Logistics 23-2077.pdf

- Realtek 23-1187.pdf

- Shockwave Medical 23-1864.pdf

- US Inventor 24-1396.pdf

STATUTORY_BARS_ON_SALE_PUBLIC_USE

- Ingenico 23-1367.pdf

- Jiaxing Super 23-1715.pdf

VENUE_TRANSFER_PERSONAL_JURISDICTION

- Focus Products 23-1446.pdf

- Regeneron 24-1965.pdf

Procedure - Preliminary Injunction

**FMC Corp. v. Sharda USA:

Sufficiency of Pleading

- Adnexus 24-1551.pdf

1)
957 F.3d 1334, 1338–40 (Fed. Cir. 2020)
2)
935 F.3d 170 (Fed. Cir. 2019)
3)
790 F.3d 1315, 1323–24 (Fed. Cir. 2015)
4)
967 F.3d 1353, 1371 (Fed. Cir. 2020)