Roche Diagnostics Operations, Inc. v. Lifescan Inc.

660 F. App'x 932
CourtCourt of Appeals for the Federal Circuit
DecidedSeptember 22, 2016
Docket2015-1356
StatusPublished

This text of 660 F. App'x 932 (Roche Diagnostics Operations, Inc. v. Lifescan Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Roche Diagnostics Operations, Inc. v. Lifescan Inc., 660 F. App'x 932 (Fed. Cir. 2016).

Opinion

Reyna, Circuit Judge.

Roche Diagnostics Operations, Inc. and Corange International Limited (“Roche”) appeal from the United States District Court for the District of Delaware’s grant of summary judgment in favor of Lifescan Incorporated and Nova Biomedical Corporation (“Defendants”). The district court entered judgment of non-infringement after construing the term “electrode” in a way that excluded Defendants’ products. The district court’s claim construction was correct and we therefore affirm the court’s judgment of non-infringement.

BACKGROUND

I. Patents

This case involves U.S. Patent Nos. 7,276,146 (“'146 patent”) and 7,276,147 (“'147 patent”). Both patents claim priority to the same provisional application and have similar specifications.1

The patents claim methods for determining the concentration of glucose in a [934]*934blood sample. Claim 1 of the '146 patent is representative of the asserted claims:

1. A method of determining the concentration of glucose in a blood sample, comprising;
providing a disposable biosensor test strip including a capillary chamber having a depth suitable for capillary flow of blood and holding a volume of between about 0.1 |xl and about 1.0 |xl of the blood sample, a working electrode and a counter or reference electrode disposed within the capillary chamber, and a reagent proximal to or in contact with at least the working electrode, the reagent including an enzyme and a mediator, the reagent reacting with glucose to produce an electroactive reaction product;
applying a blood sample containing glucose into the capillary chamber, the capillary chamber directing capillary flow of the blood sample into contact with the reagent to cause the blood sample to at least partially solubilize or hydrate the reagent;
detecting the blood sample in the capillary chamber;
following said detecting, applying or controlling the voltage or current across the working and counter or reference electrodes;
electrooxidizing or electroreducing the electroactive reaction product at the working electrode; and
within 10 seconds after said detecting, determining and providing a readout of the glucose concentration in the blood sample, said determining comprising correlating the electrooxidized or electroreduced electroactive reaction product to the concentration of glucose in the blood sample.

'146 patent col. 2911. 38-67.

II. Procedural History

Roche sued Defendants for infringement of the '146 and '147 patents. The parties disagreed about the proper construction of certain claim limitations that included the term “electrode.” Roche initially proposed constructions describing the function of particular electrodes. For example, it argued that “working electrode” should be construed as “[a]n electrode in an electrochemical cell at which the reaction of interest occurs.” J.A. 12. Roche argued that the claimed electrodes “may be of any dimension that provides useful or advantageous results with relatively small samples.” J.A. 14487. Defendants argued that the term “electrode” should be construed as “mi-croelectrode having a width of 15 to 100 ixm.”2 J.A. 12. For example, Defendants proposed that “working electrode” should be construed as “[a] working microelec-trode having a width of 15 to 100 ixm.” Id.

At a Markman hearing, Roche opposed Defendants’ “electrode” constructions, alleging, that “electrode” included not only microelectrodes but also macroelectrodes. Roche argued that the term “electrode” included certain electrodes with widths from 300 to 1,000 |xm, which Roche asserted were macroelectrodes, not microelec-trodes. Roche did not dispute that microe-lectrodes only included electrodes up to 100 |xm in width.

The district court found that the claimed electrodes were limited to microelectrodes by assertions in the shared specification about “the invention” and arguments during prosecution distinguishing prior art. Roche Diagnostics Operations, Inc. v. Ab[935]*935bott Diabetes Care, 667 F.Supp.2d 429, 435 (D. Del. 2009). It construed “electrode” to mean “microelectrode having a width of 15 (xm up to approximately 100 ¡xm.” Id. at 442-43.

Roche moved for reconsideration. While Roche conceded that the claim term “electrode” did not include macroelectrodes, Roche argued that microelectrodes included electrodes up to 1,000 ¡xm in width.

The district court denied Roche’s motion for reconsideration, but said “[i]t’s a great point for the Federal Circuit, and I actually think you might havé a point. But it will be interesting to see what they say.” J.A. 35. The court entered summary judgment of non-infringement on the basis that Defendants’ products contain electrodes larger than 100 ¡xm.

Roche appealed to this court and repeated the argument it had first raised-in its motion for reconsideration: it asserted that microelectrodes included electrodes up to 1,000 ¡xm in width. Roche Diagnostics Operations, Inc. v. Lifescan Inc., 452 Fed.Appx. 989, 994-95 (Fed. Cir. 2012) (Roche I). Defendants opposed Roche’s arguments, but did not challenge whether these arguments were properly before the court. Id. at 994-97.

As the district court had not previously addressed the parties’ arguments regarding 1,000 ¡xm microelectrodes, we declined to address them and remanded so that the district court could consider them in the first instance. Id.

On remand, the district court considered the parties’ arguments and affirmed its earlier decision that “electrode” meant “microelectrode having a width of 15 ¡xm up to approximately 100 ¡xm.” Roche Diagnostics Operations, Inc, v. Abbott Diabetes Care, Inc., No. CV 07-753-RGA, 2014 WL 6871579, at *4-6 (D. Del. Dec. 5, 2014) (“Remand Op.”).3

This appeal followed. We have jurisdiction under 28 U.S.C. § 1295(a)(1).

Discussion

Roche challenges the district court’s claim construction. We review a district court’s claim construction de novo. Teva Pharm. USA, Inc. v. Sandoz, Inc., — U.S. -, 135 S.Ct. 831, 841, — L.Ed.2d - (2015). If a district court makes factual findings about extrinsic evidence that underlie its construction, we review the factual findings for clear error. Id. at 842.

Claim terms are “generally given their ordinary and customary meaning.” Phillips v. AWH Corp., 415 F.3d 1303, 1312-13 [936]*936(Fed. Cir. 2005) (quoting Vitronics Corp. v. Conceptronic, Inc., 90 F.3d 1576, 1582 (Fed. Cir. 1996)). A term’s ordinary meaning is “its meaning to the ordinary artisan after reading the entire patent.” Id. at 1321. A specification may define claim terms expressly or by implication. Id. at 1320-21.

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