FDA applicant

Cox Medical Ent., Inc.

Ventura, CA15 decisions1991–19950 recalls

FDA records 15 decisions for Cox Medical Ent., Inc. (Ventura, CA) from 1991 to 1995: 15 510(k) clearances. Most are in product codes FEB (Accessories, Cleaning, For Endoscope) and FCL (Forceps, Biopsy, Non-Electric). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Cox Medical Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cox Medical Ent., 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?