Life Technologies Corp. v. Promega Corp.

137 S. Ct. 734, 26 Fla. L. Weekly Fed. S 434, 197 L. Ed. 2d 33, 580 U.S. 140, 2017 U.S. LEXIS 1428, 121 U.S.P.Q. 2d (BNA) 1641, 2017 WL 685531
CourtSupreme Court of the United States
DecidedFebruary 22, 2017
Docket14–1538.
StatusPublished
Cited by32 cases

This text of 137 S. Ct. 734 (Life Technologies Corp. v. Promega Corp.) is published on Counsel Stack Legal Research, covering Supreme Court of the United States primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Life Technologies Corp. v. Promega Corp., 137 S. Ct. 734, 26 Fla. L. Weekly Fed. S 434, 197 L. Ed. 2d 33, 580 U.S. 140, 2017 U.S. LEXIS 1428, 121 U.S.P.Q. 2d (BNA) 1641, 2017 WL 685531 (U.S. 2017).

Opinion

Justice SOTOMAYOR delivered the opinion of the Court.

This case concerns the intersection of international supply chains and federal patent law. Section 271(f)(1) of the Patent Act of 1952 prohibits the supply from the United States of "all or a substantial portion" of the components of a patented invention for combination abroad. 35 U.S.C. § 271 (f)(1). We granted certiorari to determine whether a party that supplies a single component of a multicomponent invention for manufacture abroad can be held liable for infringement under § 271(f)(1). 579 U.S. ----, 136 S.Ct. 2505 , 195 L.Ed.2d 838 (2016). We hold that a single component does not constitute a substantial portion of the components that can give rise to liability under § 271(f)(1). Because only a single component of the patented invention at issue here was supplied from the United States, we reverse and remand.

I

A

We begin with an overview of the patent in dispute. Although the science behind *738 the patent is complex, a basic understanding suffices to resolve the question presented by this case.

The Tautz patent, U.S. Reissue Patent No. RE 37,984, claims a toolkit for genetic testing. 1 The kit is used to take small samples of genetic material-in the form of nucleotide sequences that make up the molecule deoxyribonucleic acid (commonly referred to as "DNA")-and then synthesize multiple copies of a particular nucleotide sequence. This process of copying, known as amplification, generates DNA profiles that can be used by law enforcement agencies for forensic identification and by clinical and research institutions around the world. For purposes of this litigation, the parties agree that the kit covered by the Tautz patent contains five components: (1) a mixture of primers that mark the part of the DNA strand to be copied; (2) nucleotides for forming replicated strands of DNA; (3) an enzyme known as Taq polymerase; (4) a buffer solution for the amplification; and (5) control DNA. 2

Respondent Promega Corporation was the exclusive licensee of the Tautz patent. Petitioner Life Technologies Corporation manufactured genetic testing kits. 3 During the timeframe relevant here, Promega sublicensed the Tautz patent to Life Technologies for the manufacture and sale of the kits for use in certain licensed law enforcement fields worldwide. Life Technologies manufactured all but one component of the kits in the United Kingdom. It manufactured that component-the Taq polymerase-in the United States. Life Technologies shipped the Taq polymerase to its United Kingdom facility, where it was combined with the other four components of the kit.

Four years into the agreement, Promega sued Life Technologies on the grounds that Life Technologies had infringed the patent by selling the kits outside the licensed fields of use to clinical and research markets. As relevant here, Promega alleged that Life Technologies' supply of the Taq polymerase from the United States to its United Kingdom manufacturing facilities triggered liability under § 271(f)(1).

B

At trial, the parties disputed the scope of § 271(f)(1)'s prohibition against supplying all or a substantial portion of the components of a patented invention from the United States for combination abroad. Section 271(f)(1)' s full text reads:

"Whoever without authority supplies or causes to be supplied in or from the United States all or a substantial portion of the components of a patented invention, where such components are uncombined in whole or in part, in such manner as to actively induce the combination of such components outside of the United States in a manner that would infringe the patent if such combination occurred within the United States, shall be liable as an infringer . "

*739 The jury returned a verdict for Promega, finding that Life Technologies had willfully infringed the patent. Life Technologies then moved for judgment as a matter of law, contending that § 271(f)(1) did not apply to its conduct because the phrase "all or a substantial portion" does not encompass the supply of a single component of a multicomponent invention.

The District Court granted Life Technologies' motion. The court agreed that there could be no infringement under § 271(f)(1) because Promega's evidence at trial "showed at most that one component of all of the accused products, [the Taq ] polymerase, was supplied from the United States." 2012 WL 12862829 , *3 (W.D.Wis., Sept. 13, 2012) (Crabb, J.). Section 271(f)(1)'s reference to "a substantial portion of the components," the District Court ruled, does not embrace the supply of a single component. Id., at *5.

The Court of Appeals for the Federal Circuit reversed and reinstated the jury's verdict finding Life Technologies liable for infringement. 4 773 F.3d 1338 , 1353 (2014). As relevant here, the court held that "there are circumstances in which a party may be liable under § 271(f)(1) for supplying or causing to be supplied a single component for combination outside the United States." Ibid. The Federal Circuit concluded that the dictionary definition of "substantial" is "important" or "essential," which it read to suggest that a single important component can be a " 'substantial portion of the components' " of a patented invention. Ibid . Relying in part on expert trial testimony that the Taq polymerase is a " 'main' " and " 'major' " component of the kits, the court ruled that the single Taq polymerase component was a substantial component as the term is used in § 271(f)(1). Id., at 1356 .

II

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137 S. Ct. 734, 26 Fla. L. Weekly Fed. S 434, 197 L. Ed. 2d 33, 580 U.S. 140, 2017 U.S. LEXIS 1428, 121 U.S.P.Q. 2d (BNA) 1641, 2017 WL 685531, Counsel Stack Legal Research, https://law.counselstack.com/opinion/life-technologies-corp-v-promega-corp-scotus-2017.