throbber
Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 1 of 19 PageID #: 375
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`IN THE UNITED STATES DISTRICT COURT
`FOR THE EASTERN DISTRICT OF TEXAS
`SHERMAN DIVISION
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`OCEAN SEMICONDUCTOR LLC,
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`Plaintiff,
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`v.
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`HUAWEI DEVICE USA, INC., HUAWEI
`DEVICE CO., LTD., AND HISILICON
`TECHNOLOGIES CO., LTD.,
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`Defendants.
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`C.A. No. 4:20-cv-00991-ALM
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`DEMAND FOR JURY TRIAL
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`PLAINTIFF OCEAN SEMICONDUCTOR LLC’S OPPOSITION
`TO DEFENDANTS’ MOTION
`TO DISMISS FOR FAILURE TO STATE A CLAIM UNDER 35 U.S.C. § 271(g)
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`Dated: April 19, 2021
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`DEVLIN LAW FIRM LLC
`Timothy Devlin
`tdevlin@devlinlawfirm.com
`Henrik Parker (pro hac vice forthcoming)
`hparker@devlinlawfirm.com
`Alex Chan
`State Bar No. 24108051
`achan@devlinlawfirm.com
`1526 Gilpin Avenue
`Wilmington, DE 19806
`Telephone: (302) 449-9010
`Facsimile: (302) 353-4251
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`Attorneys for Plaintiff
`Ocean Semiconductor LLP
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`1
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 2 of 19 PageID #: 376
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`TABLE OF CONTENTS
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`I.
`
`INTRODUCTION ................................................................................................................... 1
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`II.
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`LEGAL STANDARD .......................................................................................................... 1
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`A. The High Bar for a Motion to Dismiss ................................................................................ 1
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`B. The Broad Reach of Infringement Under 35 U.S.C. § 271(g) ............................................. 2
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`III. ARGUMENT ....................................................................................................................... 3
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`A. The Methods of the ’402 Patent Involve the Making of Physical Products Such as Silicon
`Wafers, and Ocean’s Pleadings Reflect that Fact ....................................................................... 4
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`1. The Intrinsic Record Amply Shows that Physical Products Are Being Manufactured ... 4
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`2. Huawei’s Argument Fails Because There Is No Legitimate Dispute that Each Claimed
`Limitation is Performed During the Manufacture of Physical Products ................................. 5
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`3. Huawei’s Arguments Are Not Supported by Bayer or Momenta .................................... 6
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`B. The Methods of the ’538 Patent Involve the Making of Physical Products Such as Silicon
`Wafers, and Ocean’s Pleadings Reflect that Fact ....................................................................... 7
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`1. Huawei’s Arguments Are Not Supported by Bayer or Momenta .................................... 9
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`2. Huawei Omits Key Claim Elements that Unmistakably Cover the Manufacture of
`Physical Products .................................................................................................................. 10
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`C. The Methods of the ’305 and ’248 Patents Involve the Making of Physical Products Such
`as Silicon Wafers, and Ocean’s Pleadings Reflect that Fact .................................................... 10
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`D. In All Events, Fact Issues Preclude Dismissal ................................................................... 13
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`E. At Worst, Rather Than Dismissing the Complaint, Leave to Amend Should Be Granted 14
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`IV. CONCLUSION .................................................................................................................. 14
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`i
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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 3 of 19 PageID #: 377
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`TABLE OF AUTHORITIES
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`Page(s)
`
`Cases
`
`Ashcroft v. Iqbal
`556 U.S. 662 (2009) .................................................................................................................... 1
`
`Bayer AG v. Housey Pharm., Inc.,
`340 F.3d 1367, 1368 (Fed. Cir. 2003)................................................................................ passim
`
`Bell Atl. Corp. v. Twombly
`550 U.S. 544 (2007) ................................................................................................................ 1, 2
`
`Biotec Biologische Naturverpackungen GmbH & Co. v. Biocorp, Inc.,
`249 F.3d 1341 (Fed. Cir. 2001)................................................................................................. 15
`
`Bio-Technology General Corp. v. Genentech, Inc.,
`80 F.3d 1553 (Fed. Cir. 1996)........................................................................................... 4, 8, 14
`
`Bustos v. Martini Club, Inc.,
`599 F.3d 458 (5th Cir. 2010) ...................................................................................................... 2
`
`Causey v. Sewell Cadillac-Chevrolet, Inc.
`394 F.3d 285 (5th Cir. 2004) ...................................................................................................... 2
`
`Disc Disease Sols. Inc. v. VGH Sols., Inc.
`888 F.3 1256 (Fed. Cir. 2018)..................................................................................................... 3
`
`Eli Lilly & Co. v. Am. Cyanamid Co.,
`82 F.3d 1568 (Fed. Cir. 1996)........................................................................................... 3, 4, 14
`
`Encoditech, LLC v. Citizen Watch Co. of Am.
`C.A. No. 18-1335-XR, 2019 U.S. Dist. LEXIS 105833 (W.D. Tex. June 25, 2019) ................. 3
`
`Frye v. Anadarko Petro. Corp.,
`953 F.3d 285 (5th Cir. 2019) ....................................................................................................... 2
`
`Griggs v. Hinds Junior Coll.,
`563 F.2d 179 (5th Cir. 1977) .................................................................................................... 16
`
`Lone Star Motor Imp., Inc. v. Citroen Cars Corp.,
`288 F.2d 69 (5th Cir. 1961) ...................................................................................................... 16
`
`Lormand v. US Unwired, Inc.,
`565 F.3d 228 (5th Cir. 2009) ....................................................................................................... 2
`
`Millennium Cryogenic Techs., Ltd. v. Weatherford Artificial Lift Sys.,
`Civil Action No. H-12-0890-KPE,
`2012 U.S. Dist. LEXIS 196638 (S.D. Tex. 2012) .................................................................... 15
`
`Momenta Pharms., Inc. v. Teva Pharms. USA Inc.,
`809 F.3d 610 (Fed. Cir. 2015)..................................................................................................... 9
`
`Ormco Corp. v. Align Tech., Inc.,
`653 F. Supp. 2d 1016 (C.D. Cal. 2009) .............................................................................. 14, 15
`
`ii
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 4 of 19 PageID #: 378
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`Skinner v. Switzer
`562 U.S. 521 (2011) .................................................................................................................... 2
`
`Zond, LLC v. Renesas Elecs. Corp.,
`Civil Action No. 13-11625-NMG,
`2014 U.S. Dist. LEXIS 114363 (D. Mass. Aug. 15, 2014)....................................................... 15
`
`
`
`Statutes
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`35 U.S.C. § 271 ............................................................................................................................... 2
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`Rules
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`Fed. R. Civ. P. 15 .......................................................................................................................... 14
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`iii
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 5 of 19 PageID #: 379
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`I.
`
`INTRODUCTION
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`The Motion to Dismiss (Dkt. 13) filed by by defendants Huawei Device USA, Inc.,
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`Huawei Device Co., Ltd., and HiSilicon Technologies Co., Ltd. (collectively “Huawei”), which
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`is essentially a replica of a Rule 12(b) motion filed by NXP—a defendant in a parallel action
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`pending in the Western District of Texas (Ocean Semicondcutor LLC. V. NXP Semiconductors
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`N.V. et al., No. 6:20-cv-1212-ADA (W.D. Tex.), misconstrues both the nature of the patents at
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`issue and the applicable law. Each of the four patents asserted by Ocean Semiconductor LLC
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`(“Ocean”) in this action that Huawei seeks to dismiss—U.S. Patent Nos. 6,725,402 (“’402
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`patent”), 8,676,538 (“’538 patent”), 6,907,305 (“’305 patent”), and 6,968,248 (“’248 patent”)
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`(collectively “Asserted Patents”)—describes the manufacturing of semiconductors in
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`excruciating detail and claims methods used for, and during, that manufacturing used, for
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`example, to manufacture semiconductor wafers—physical products falling squarely within the
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`scope of § 271(g). Huawei’s bare bones motion, which includes little factual or legal argument,
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`coupled with Huawei’s (a) artificial attempt to limit the Court’s analysis to isolated claimed
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`features; and (b) misapplication of the relevant law, falls far short of the high bar necessary to
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`obtain dismissal. In all events, fact issues preclude dismissal and the Motion should be denied.
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`II.
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`LEGAL STANDARD
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`A.
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`The High Bar for a Motion to Dismiss
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`Under Federal Rule of Civil Procedure 12(b)(6), dismissal of a complaint or cause of
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`action is appropriate if it fails to state a claim for relief that is “plausible on its face.” Ashcroft v.
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`Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570 (2007)).
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`When considering a motion to dismiss under Rule 12(b)(6), “[t]he court must accept all well-
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`pleaded facts as true and must draw all reasonable inferences in favor of the plaintiff.” Frye v.
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`Anadarko Petro. Corp., 953 F.3d 285, 290-91 (5th Cir. 2019) (citing Lormand v. US Unwired,
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`1
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 6 of 19 PageID #: 380
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`Inc., 565 F.3d 228, 232 (5th Cir. 2009));1 see also Bustos v. Martini Club, Inc., 599 F.3d 458, 461
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`(5th Cir. 2010) (internal quotations omitted); see also Bell Atl. Corp., 550 U.S. at 570. The
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`question resolved is “whether [the] complaint was sufficient to cross the federal court’s
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`threshold”—not whether the plaintiff will ultimately prevail. Skinner v. Switzer, 562 U.S. 521,
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`530 (2011). Pleadings should be construed broadly in light of the allegations as a whole, and the
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`facts pled should be viewed expansively in light of the liberal pleading standards. See, e.g.,
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`Causey v. Sewell Cadillac-Chevrolet, Inc., 394 F.3d 285, 288-90 (5th Cir. 2004).
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`This Court has held, based on Federal Circuit precedent, that identification of specific
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`products, when coupled with allegations that defendants make, sell, offer to sell, import or use
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`the accused products in the United States the accused products and that each accused product
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`satisfies each and every limitation of at least one patent claim is enough to meet “the relatively
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`low threshold for stating a claim for patent infringement.” Encoditech, LLC v. Citizen Watch Co.
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`of Am., C.A. No. 18-1335-XR, 2019 U.S. Dist. LEXIS 105833, at *10 (W.D. Tex. June 25, 2019)
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`(citing Disc Disease Sols. Inc. v. VGH Sols., Inc., 888 F.3 1256 (Fed. Cir. 2018)).
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`B.
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`The Broad Reach of Infringement Under 35 U.S.C. § 271(g)
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`Section 271(g) attaches liability to the import, use, sale, or offer for sale of products made
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`by a patented process. “By enacting the Process Patent Amendments Act, the principal portion
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`of which is codified as 35 U.S.C. § 271(g), Congress changed the law by making it an act of
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`infringement to import into the United States, or to sell or use within the United States ‘a product
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`which is made by a process patented in the United States[.]’” Eli Lilly & Co. v. Am. Cyanamid
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`Co., 82 F.3d 1568, 1572 (Fed. Cir. 1996).
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`Congress created liability under § 271(g) to ensure that holders of process patents and
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`domestic manufacturers were not disadvantaged relative to holders of device and system claims
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`1 Unless otherwise indicated, all emphasis in this brief has been added.
`2
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 7 of 19 PageID #: 381
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`or foreign manufacturers, and the courts interpret “made by” in view of these policy goals.
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`Bayer AG v. Housey Pharm., Inc., 340 F.3d 1367, 1368, 1373 (Fed. Cir. 2003); Bio-Technology
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`General Corp. v. Genentech, Inc., 80 F.3d 1553, 1561 (Fed. Cir. 1996), cert. denied, 519 U.S.
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`911 (1996); Eli Lilly & Co. 82 F.3d at 1578; 5 Chisum on Patents § 16.02[6][d][iv] (2019). The
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`Federal Circuit has interpreted the term “made” as used in § 271(g) to mean “manufactured” and
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`the term “product” to mean a “physical article.” Bayer, 340 F.3d at 1377.
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`Section 271(g) is applied broadly. When enacting the Process Patent Amendments Act
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`(“PPAA”), Congress specifically declined to require that a product be made “directly” from a
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`patented process in order to infringe under § 271(g). See Eli Lilly & Co., 82 F.3d at 1576. “In
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`enacting the PPAA, Congress did not include a positive definition of ‘made by.’ The court must
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`interpret ‘made by’ in light of the PPAA’s policy to afford meaningful protection for owners of
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`patents claiming processes.” 5 Chisum on Patents § 16.02[6][d][iv] (2019) (citing Bayer, 340
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`F.3d at 1368; Bio-Technology General Corp., 80 F.3d at 1561). “The connection between a
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`patented process and a product can vary from immediate . . . to remote[.]” 5 Chisum on Patents
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`§ 16.02[6][d][iv] (2019).
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`Consequently, whether a product is “made by” a patent should be interpreted expansively
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`to include products made through the “agency,” “efficacy,” “work,” “participation,” “means or
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`instrumentality,” “medium,” or “operation” of a process. Bayer, 340 F.3d at 1378, n.12 (citing
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`Webster’s and Random House dictionaries).
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`III. ARGUMENT
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`Contrary to Huawei’s misdirection and simplistic, conclusory allegations, each of the
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`four patents at issue claims methods that relate directly to the making of physical products. As
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`such, Ocean properly pleaded causes of action under § 271(g) as to each of those patents. In all
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`events, fact issues preclude dismissal at this early stage.
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`3
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 8 of 19 PageID #: 382
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`A.
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`The Methods of the ’402 Patent Involve the Making of Physical Products
`Such as Silicon Wafers, and Ocean’s Pleadings Reflect that Fact
`
`1.
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`The Intrinsic Record Amply Shows that Physical Products Are Being
`Manufactured
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`Contrary to Huawei’s contention,2 the ’402 patent itself confirms that the claimed
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`invention directly relates to: (1) the making of physical products such as silicon wafers; and (2)
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`the actual manufacture of such products. For example, the exemplary system and its
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`manufacturing tools are “semiconductor fabrication equipment used to produce a processing
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`piece, such as a silicon wafer,” and the exemplary tool is a “Rapid Thermal Processing (RTP)
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`tool” or “a tool for processing silicon wafers.” (Dkt. 1-3 (’402 patent) at 2:42-48.) The
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`independent method claim recites “the manufacture of a processing piece”; and the independent
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`system claim recites a tool adapted to “manufacture a processing piece” (claim 8). One
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`dependent claim recites that “the processing piece is a silicon wafer” (claim 14).
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`Ocean’s pleading allegations are consistent with the ’402 patent’s focus on physical
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`articles, in particular semiconductor products made by Huawei and its contract suppliers. In
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`particular, the Complaint limits its accusations under § 271(g) to products made using the
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`claimed method—expressly alleging that “Huawei has directly infringed and continues to
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`infringe at least claim 1 of the ’402 patent . . . by importing into the United States, and/or using,
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`and/or selling, and/or offering for sale in the United States, without authority or license, the ’402
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`Accused Products, in violation of 35 U.S.C. § 271(g).” (Dkt. 1 at ¶ 94.)
`
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`2 Notably, one of the other defendants—NVIDIA—in parallel actions pending in the Western
`District of Texas (Ocean Semicondcutor LLC. V. NVIDIA Corporation, No. 6:20-cv-1211-ADA
`(W.D.Tex.)) who previously filed motions to dismiss litigation (see Dkt. 13 at 1 n.2) does not
`challenge the applicability of § 271(g) to the ’402 patent while challenging that section’s
`applicability to the other three patents here at issue, thus implicitly recognizing that Huawei’s
`argument here has no merit. (See Ex. 1 to the co-filed Declaration of Alex Chan in Support of
`Plaintiff’s Brief in Opposition to Defendant’s Motion to Dismiss Under 35 U.S.C. § 271(g), at ¶
`4.)
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`4
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 9 of 19 PageID #: 383
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`2.
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`Huawei’s Argument Fails Because There Is No Legitimate Dispute
`that Each Claimed Limitation is Performed During the Manufacture
`of Physical Products
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`Apparently recognizing that Ocean clearly accuses products falling with the scope of §
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`271(g), Huawei relies solely on a misguided contention that “claim 1 produces only information –
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`notification of the existence of a fault condition.” (Dkt. 13 at 3.) Huawei’s argument, however, is
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`premised on a deliberate misreading of what the ’402 patent actually describes and claims—a
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`process for manufacturing physical products (“processing pieces”) such as silicon wafers. The
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`patent claims themselves demonstrate this fact.
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`Specifically, the patented system receives “operational state data of a processing tool”
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`(e.g., recited as “receiving . . .operational state data of a processing tool related to the
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`manufacture of a processing piece” in claim 1) “when the tool 105 is operating and processing a
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`given wafer,” and sends data to a fault detection unit (e.g., recited as “sending the translated state
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`data from the data collection unit to the fault detection unit in claim 1) “while the particular
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`wafer is being processed” to ensure that the tool is operating “within acceptable operational
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`limits (Dkt. 1-3 (’402 patent) at 3:27-31; 4:3-7.) If the processing tool is operating within
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`appropriate parameters, manufacturing proceeds (e.g., recited as “determining if a fault condition
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`exists with the processing tool” in claim 1). If a “fault condition” is detected, the system can act
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`to adjust the manufacturing process in a variety of ways, including: “manipulate the tool,” (id. at
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`5:18-20); “shut down the tool,” (id. at 5:65-6:4); or “apprise a technician of any potential
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`solutions to rectify the fault condition” (id. at 6:4-9) (e.g., recited in claim 1 as “performing a
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`predetermined action on the processing tool in response to the presence of a fault condition”).
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`Where the system is monitoring tools but detects no fault, manufacturing can continue as normal.
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`All of these activities, and the recited limitations, relate directly to the manufacture of
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`the physical products and the language of claim 1 readily reflects these activities. Thus,
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`5
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 10 of 19 PageID #: 384
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`Huawei’s narrow interpretation of § 271(g) misses the mark. The target of § 271(g) is the
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`importation of a product made using a patented process or subsequent use, sale, or offer for sale
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`of that product within the United States. Bayer, 340 F.3d at 1375. While the statute requires a
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`physical product, the offending physical product is that which was manufactured using the
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`patented process. (Id. at 1377.) In that context, what is important here is not the “notification of
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`the existence of a fault condition” (Dkt. 13 at 3) in isolation, as has been phrased by Huawei, but
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`the use of that process in the manufacturing of the physical products later imported into, for use,
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`sale, or offer for sale in, the United States.
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`Ocean’s Complaint alleges that Huawei used (and still uses) the patented processes,
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`including all of the limitations of claim 1, as part of the manufacture of Huawei’s accused
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`products. (See, e.g., Dkt. 1 at ¶ 92: “The ’402 Accused Products are manufactured by a process
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`including all of the limitations of at least claim 1 of the ’402 patent. Each such product includes
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`an integrated circuit fabricated or manufactured using, for example, the Applied Materials E3
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`system and/or PDF Solutions’ Exensio system.”). In other words, a semiconductor physical
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`product, such as a silicon wafer, made by a manufacturing tool that uses the patented fault
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`detection method to identify manufacturing faults is a product “made by” a patented process for
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`detecting such faults. This is the exact type of conduct prohibited by § 271(g). Bio-Tech. Gen.
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`Corp., 80 F.3d at 1561 (holding that a protein made by a host organism expressing an inserted
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`plasmid was a product “made by” a patented process for creating the plasmid).
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`3.
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`Huawei’s Arguments Are Not Supported by Bayer or Momenta
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`While Huawei cites to Bayer and Momenta as allegedly supportive of its contentions, a
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`proper analysis reveals just the contrary.
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`First, as set out in Ocean’s Complaint, the determination of fault conditions and the
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`performance of a corrective action are crucial steps in the manufacture of Huawei’s
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`6
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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 11 of 19 PageID #: 385
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`semiconductors, unlike the generation of information in Bayer—information that was not part of
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`the manufacture of the drug products accused of infringement. Section 271(g) is thus implicated
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`here (unlike in Bayer) because the patented method is used to manufacture the alleged infringing
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`products. Consequently, Huawei’s assertion that the ’402 patent claims a process “for testing
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`final products or intermediate substances to ensure that the intended product or substance has in
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`fact been made” (Dkt. 13 at 6), is demonstrably incorrect.3
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`Second, Momenta involved a testing process that was performed on a sampling of
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`intermediate products—a process used to destroy and discard samples on which the tests were
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`performed. Momenta Pharms., Inc. v. Teva Pharms. USA Inc., 809 F.3d 610, 616-17 (Fed. Cir.
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`2015). As a result, there could never be any subsequent sale of any product on which the
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`claimed method had been performed: only products on which the claimed method had not been
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`performed survived to be developed into final products that were imported and sold. Here,
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`however, the patented method of the ’402 patent is performed during manufacturing and on all
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`wafers, and thus is actually utilized on the same units of accused products later imported and
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`used, sold, or offered for sale by Huawei. Momenta is inapposite.
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`B.
`
`The Methods of the ’538 Patent Involve the Making of Physical Products
`Such as Silicon Wafers, and Ocean’s Pleadings Reflect that Fact
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`The ’538 patent covers similar subject matter to the ’402 patent—i.e., fault detection and
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`its use in the operation of a tool manufacturing semiconductor wafers. As such, Huawei’s
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`contentions as to the ’538 patent suffer from all of the same flaws discussed above with respect
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`to the ’402 patent.
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`3 While Huawei quotes from Bayer (Dkt. 13 at 2), it truncates the quote to blur the full meaning.
`The full quotation reads: “Thus, the process must be used directly in the manufacture of the
`product, and not merely as a predicate process to identify the product to be manufactured.” Bayer,
`340 F.3d at 1378. Certainly, the processes claimed in the patents at issue here are not used simply
`“to identify the product to be manufactured.”
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`7
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 12 of 19 PageID #: 386
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`Like the ’402 patent, the ’538 patent claims “[a] method, comprising: performing in a
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`computer a fault detection analysis relating to processing of a workpiece.” (Dkt. 1-7 (’538
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`patent) at 13:28-30.) This “workpiece comprises a semiconductor wafer.” (Claim 2.) The fault
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`detection analysis includes determining “a relationship of a parameter relating to said fault
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`detection analysis to a detected fault,” including a relationship between at least one of
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`“pressure,” “temperature,” “data,” “humidity,” or “gas flow.” (See claim 9.) The performance
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`of the fault detection method is not undertaken for mere testing or data collection purposes, but
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`rather “relat[es] to processing of a subsequent workpiece. . . .” (Id. at 13:38.) Thus, on its face,
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`the method of claim 1 is one directly implicating the manufacture of semiconductor wafers.
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`This is confirmed by the specification, which further delineates the ways in which the
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`patented methods involve not only collection and analysis of key manufacturing data from the
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`manufacturing process, but also control of manufacturing tools used for manufacturing
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`semiconductor wafers.4 For example, as part of the weighting process, “the processing system
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`may perform subsequent processes upon the semiconductor wafers based upon the newly
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`adjusted parameter-weighting. . . .” (Id. at 11:7-9.) Figure 7 similarly indicates that the
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`“perform subsequent process step” follows the “perform dynamic PCA weighting process” step.
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`(Id. at Fig. 7.)
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`The specification also illustrates that fault detection is an integral part of the
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`manufacturing process, not a function that occurs at a spatial or temporal remove. For example,
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`“[t]he system 300 also comprises a fault detection unit 380, which is capable of performing
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`various fault detection associated with the processing tool 310 when processing the
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`semiconductor wafers 105.” (Id. at 7:3-6.) Similarly, “in some embodiments . . . the control
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`4 Claims are always construed in light of the entirety of the patent’s disclosure, including the
`specification and other claims. Phillips v. AWH Corp., 415 F.3d 1303, 1314 (Fed. Cir. 2005).
`8
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`

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`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 13 of 19 PageID #: 387
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`strategies taught by the present invention can be applied to virtually any of the semiconductor
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`manufacturing tools on the factory floor.” (Id. at 12:52-61.)
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`Indeed, the ability to improve the functioning of process tools is among the principal
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`benefits cited in the patent. For example, by “utilizing embodiments of the present invention, a
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`more effective and accurate process adjustment may be performed to achieve more accurate
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`semiconductor wafer 105 characteristics and improved yields.” (Id. at 12:47-51.)
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`1.
`
`Huawei’s Arguments Are Not Supported by Bayer or Momenta
`
`As with claim 1 of the ’402 patent, Huawei wrongly contends that “claim 1 [of the ’538
`
`patent] covers adjusting a parameter used for fault detection to perform fault detection using the
`
`adjusted parameter – all of which is informational.” (Dkt. 13 at 4.) In other words, Huawei
`
`argues that § 271(g) liability only attaches where the patented method directly claims the
`
`physical manufacture of that product. But the cases cited by Huawei provide no such support.
`
`In particular, Bayer relates to the question of whether information developed using a
`
`patented process is a “product” within the scope of § 271(g), such that importation of that
`
`information is an infringement. Bayer, 340 F.3d at 1370-71. The court in Bayer held that the
`
`importation of information was not importation of a “product,” because information is not
`
`“manufactured” at all. (Id. at 1377.) Here, on the other hand, what is imported is not
`
`information, but rather the physical products manufactured using these patented processes.
`
`Notably, Bayer itself articulates this very distinction, plainly demonstrating why the
`
`asserted patents in this case are all within the scope of § 271(g). The Bayer court separately
`
`analyzed claims involving a physical drug, holding that it “is beyond dispute that a drug is a
`
`physical product that has been manufactured.” (Id.) As with the drug in Bayer, it is beyond
`
`legitimate dispute that the semiconductor wafers described in the ’538 patent, and the products
`
`9
`
`

`

`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 14 of 19 PageID #: 388
`
`alleged to infringe, are physical products, and that the claimed methods of the ’538 patent relate
`
`directly to the manufacture of such products.
`
`Huawei is also wrong to the extent that it argues that the ’538 patent claims a method for
`
`“testing of the process for manufacturing the accused products” (Dkt. 13 at 6) as in Momenta.
`
`As was discussed above with respect to the ’402 patent, the ’538 method is performed during
`
`manufacture and on all wafers.
`
`2.
`
`Huawei Omits Key Claim Elements that Unmistakably Cover the
`Manufacture of Physical Products
`
`In alleging that claim 1 of the ’538 patent covers only “adjusting a parameter used for
`
`fault detection to perform fault detection using the adjusted parameter” (Dkt. 13 at 4), Huawei
`
`inappropriately omits key claim elements that expressly recite the physical nature of the products
`
`being manufactured. For example, as stated above, claim 1 recites the “processing of a
`
`workpiece” as well as “processing of a subsequent workpiece” where the “workpiece comprises
`
`a semiconductor wafer.” Huawei’s motion, however, left off these key claim limitations,
`
`deliberately choosing to use ellipses to conceal those elements from the Court. (Id. at 4.) In
`
`doing so, Huawei failed to explain why or how those limitations are not implicated under §
`
`271(g).
`
`Nor did Huawei articulate any explanation as to why those key elements in combination
`
`with the remaining limitations are not used to manufacture physical articles such as
`
`semiconductor wafers.
`
`C.
`
`The Methods of the ’305 and ’248 Patents Involve the Making of Physical
`Products Such as Silicon Wafers, and Ocean’s Pleadings Reflect that Fact
`
`Huawei construes the claimed invention of the ’305 and ’248 patents as “scheduling of an
`
`action from the software scheduling agent” (Dkt. 13 at 5) but then ignores the fact that
`
`scheduling semiconductor fabrication processes is an indispensable part of semiconductor
`
`10
`
`

`

`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 15 of 19 PageID #: 389
`
`manufacturing. Without a means of scheduling, for example, semiconductor lots and individual
`
`wafers for production, it would be impossible to coordinate the complex operational steps and
`
`multiple tools used in a manufacturing facility. As such, Huawei’s contention that these patents
`
`do not claim methods used in the manufacturing of physical articles—and particularly its
`
`assertion that the claims of these patents “output information” (Dkt. 13 at 4)—are wrong.
`
`As discussed in the specifications, the semiconductor fabrication process “involves
`
`processing a number of wafers through a series of fabrication tools” in which “[l]ayers of
`
`materials are added to, removed from, and/or treated on a semiconducting substrate during
`
`fabrication to create the integrated circuits.” (Dkt. 1-2 (’305 patent) at 1:38-42; Dkt. 1-4 (’248
`
`patent) at 1:41-45.) “Efficient management of a facility for manufacturing products such as
`
`semiconductor chips requires monitoring various aspects of the manufacturing process” and
`
`“track[ing] the amount of raw materials on hand, the status of work-in-process and the status and
`
`availability of machines and tools at every step in the process.” (Dkt. 1-2 at 2:10-16; Dkt. 1-4 at
`
`2:12-18.)
`
`The ’305 and ’248 patents both describe ways “for efficiently scheduling and controlling
`
`the lots [] of wafers [] through the fabrication process,” such as “schedul[ing] ahead for each lot
`
`[] one or more operations on a specified qualified process tool 115, including . . . making
`
`optimizing decisions such as running an incomplete batch as opposed to waiting for an
`
`approaching lot,” and “schedule[ing] and initiat[ing] activities such as lot transport and
`
`processing.” (Dkt. 1-2 at 6:45-48 and 6:65-7:11; Dkt. 1-4 at 6:47-50 and 6:67-7:13.) As is
`
`evident, each of these processes is more than just “scheduling of an action.” (Dkt. 13 at 5.)
`
`This teaching is not limited to the specification; it is also manifested in the claims
`
`themselves. For example, each claim 1 of the ’305 and ’248 patents recites “a method for
`
`scheduling in an automated manufacturing environment,” including “automatically detecting
`
`11
`
`

`

`Case 4:20-cv-00991-ALM Document 14 Filed 04/19/21 Page 16 of 19 PageID #: 390
`
`an occurrence of a predetermined event in an integrated, automated process flow,” which is a
`
`“process flow [for] fabricat[ing] semiconductor devices.” (Dkt. 1-2 at 5:3-4; Dkt. 1-4 at 5:5-6.)
`
`This “process flow comprises a portion of a semiconductor manufacturing facility.” (See Claim
`
`43 of the ’305 patent.) Several of the dependent claims also elaborate on the types of events
`
`detected during manufacturing at the “semiconductor manufacturing facility.”
`
`For example, cla

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