FDA applicant

Zymetx, Inc.

Oklahoma City, OK4 decisions1996–19990 recalls

FDA records 4 decisions for Zymetx, Inc. (Oklahoma City, OK) from 1996 to 1999: 4 510(k) clearances. Most are in product codes GNX (Antigens, Cf (Including Cf Control), Influenza…) and GNR (Antisera, Neutralization, Influenza Virus A…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Zymetx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zymetx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Zymetx, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Zymetx, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Zymetx, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?