FDA applicant

Medtex Laboratories, Inc.

Seattle, WA1 decision1996–19960 recalls

FDA records 1 decision for Medtex Laboratories, Inc. (Seattle, WA) in 1996: 1 510(k) clearance. All are in product code JSX (Kit, Identification, Neisseria Gonorrhoeae). 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 Medtex Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtex Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medtex Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?