Moxness Products, Inc. v. Xomed, Inc., Defendant/cross-Appellant

891 F.2d 890, 1989 WL 146295
CourtCourt of Appeals for the Federal Circuit
DecidedJanuary 31, 1990
Docket88-1609, 89-1008
StatusPublished
Cited by9 cases

This text of 891 F.2d 890 (Moxness Products, Inc. v. Xomed, Inc., Defendant/cross-Appellant) 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
Moxness Products, Inc. v. Xomed, Inc., Defendant/cross-Appellant, 891 F.2d 890, 1989 WL 146295 (Fed. Cir. 1990).

Opinion

BISSELL, Circuit Judge.

Moxness Products, Inc. (Moxness) appeals the order of the United States District Court for the Middle District of Florida, Moxness Prods., Inc. v. Xomed, Inc., 8 USPQ2d 1281 (M.D.Fla.1988), granting judgment notwithstanding the verdict (JNOV), holding that United States Patent No. 3,807,409 (’409) is invalid for on-sale activity and public use, and granting a conditional new trial on those issues. Xomed, Inc. (Xomed) cross-appeals the adverse rulings on enforceability, estoppel, JNOV and new trial. We reverse-in-part, remand-in-part, and affirm-in-part.

BACKGROUND *

The ’409 patent relates to an ear ventilation tube used to treat medical problems of the middle ear. The patented product is known as the “Paparella ventilation tube,” honoring one of its three co-inventors, Dr. Michael Paparella.

On August 31, 1972, Dr. Paparella, Dr. Edward Goldberg, and Ralph Ostensen filed the application that issued as the ’409 patent in 1974. Medical Products Corporation (MPC), a medical devices designer and manufacturer and assignee of the ’409 patent, and Moxness, a silicone rubber manufacturer and subsequent successor in interest to the ’409 patent, formed a joint venture to produce the Paparella tubes.

Moxness, through its predecessor in interest, E.T. Manufacturing Co., Inc., initiated suit against Xomed in 1985 for infringement of the ’409 patent. The district court entered partial summary judgments that Xomed’s Type I and II ventilation tubes infringed the ’409 patent, see E.T. Mfg. Co. v. Xomed Inc., 695 F.Supp. 530, 533, 6 USPQ2d 1894, 1896 (M.D.Fla.1987), and that Moxness was barred by laches from recovering damages prior to filing suit, see E.T. Mfg. Co. v. Xomed Inc., 679 F.Supp. 1082, 1087, 4 USPQ2d 1627, 1630 (M.D.Fla.1987). Then the issues of validity, intent and materiality underlying en- *892 foreeability, willfulness, and damages were tried before a jury. The jury returned special verdicts finding that Xomed had failed to prove by clear and convincing evidence that (1) the claimed tubes were in public use or on sale prior to the critical date, (2) the claimed invention would have been obvious, and (3) the patent applicants or their attorneys had intentionally made material misrepresentations to the United States Patent and Trademark Office (PTO). The jury also found that (4) Xomed’s infringement was not willful, (5) no lost profits damages were sustained, and (6) 20% of Xomed’s Type I and II tube sales represented a reasonable royalty.

The district court entered judgment on the jury’s special verdicts and denied Xomed’s motions asserting estoppel and unenforceability for inequitable conduct. See Moxness, 8 USPQ2d at 1299-1305. In response to Xomed’s other motions, the district court (1) granted JNOV, holding the patent invalid under 35 U.S.C. § 102(b) (1982) for public use and MPC’s on-sale activity, (2) granted a conditional new trial on those issues, (3) denied JNOV on obviousness, and (4) denied a new trial on the reasonable royalty issue. See id. at 1282-96.

ISSUES

1. Whether the district court erred in granting JNOV that the patent is invalid under 35 U.S.C. § 102(b) for MPC’s on-sale activity or public use.

2. Whether the district court erred in granting a conditional new trial regarding the on-sale and public use issues.

3. Whether the district court erred in its rulings adverse to Xomed on enforceability, estoppel, JNOV and new trial.

OPINION

I. Judgment Notwithstanding the Verdict

In reviewing the district court’s disposition of the motions for JNOV, we apply the standard articulated by the Eleventh Circuit. See Sjolund v. Musland, 847 F.2d 1573, 1576, 6 USPQ2d 2020, 2023 (Fed.Cir. 1988) (applying the law of the forum in which the suit arose to review a JNOV). “[T]he court should consider all the evidence in a light most favorable to the non-movant and grant a judgment n.o.v. only if the facts and inferences point overwhelmingly in favor of the movant such that there can be but one reasonable conclusion.” Landsman Packing Co. v. Continental Can Co., 864 F.2d 721, 732 (11th Cir.1989). The trial court cannot consider the credibility of witnesses or weigh the evidence. Watts v. Great Atl. & Pac. Tea Co., 842 F.2d 307, 310 n. 5 (11th Cir.1988); 9 C.A. Wright & A.R. Miller, Federal Practice and Procedure (Wright & Miller) § 2527, at 560 (1971 & Supp.1989).

A. JNOV — On Sale

A patent is not valid if the invention was “in public use or on sale in this country, more than one year prior to the date of the application for patent in the United States.” 35 U.S.C. § 102(b). The jury returned a verdict finding that the Paparella tube covered by the patent claims was not on sale prior to August 31, 1971, the statutory bar date in this case. The district court granted JNOV, based on its conclusion that In re Theis, 610 F.2d 786, 792, 204 USPQ 188, 193 (CCPA 1979), compelled it to give no weight to certain testimony supporting the jury’s verdict. This was reversible error.

The discredited testimony was that of Dr. Goldberg, the joint venture’s medical director, who testified that a July 26, 1971, letter from G.D. Searle & Co. Ltd. to MPC was not an “order” but a “request” for Paparella tubes for developmental purposes. Mr. Ostensen, MPC’s president in 1971, had characterized the letter as an “order” for Paparella tubes, and stated his belief that the “order” had been filled. In considering Xomed’s JNOV motion, the district court explicitly “re-examined ... Dr. Goldberg’s testimony” and, based on Theis, ruled that the contradictory “oral testimony of Dr. Goldberg [could] be given no weight” because neither the letter nor Mr. Ostensen’s related correspondence mentioned developmental purposes for the Pa- *893 parella tubes. The court further concluded that other documentary evidence “preclude[d] giving counter-balancing weight to Dr. Goldberg’s oral testimony.”

The district court erred in ruling that Theis required it, as a matter of law, to assign no weight to Dr. Goldberg’s testimony when considering the motion for JNOV. While the PTO Board of Appeals (Board) in Theis refused to give any weight to an affidavit statement regarding experimental use that conflicted with documentary evidence, that case did not involve a JNOV motion. Theis,

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