FDA applicant

W. J. Medical Instruments, Inc.

Newbury Park, CA3 decisions1993–19942 recalls

FDA records 3 decisions for W. J. Medical Instruments, Inc. (Newbury Park, CA) from 1993 to 1994: 3 510(k) clearances. Most are in product codes KNF (Coagulator-Cutter, Endoscopic, Unipolar (And…) and FCX (Insufflator, Automatic Carbon-Dioxide For…). 2 recalls are linked to its devices.

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

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided W. J. Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for W. J. Medical Instruments, Inc. since 2007.

Recalls per year

2in 2007

2007high 2 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

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W. J. Medical Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?