FDA applicant

Cox Sterile Products, Inc.

Dallas, TX4 decisions1987–19940 recalls

FDA records 4 decisions for Cox Sterile Products, Inc. (Dallas, TX) from 1987 to 1994: 4 510(k) clearances. Most are in product codes KMH (Sterilizer, Dry Heat) and KCT (Sterilization Wrap Containers, Trays…). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Cox Sterile Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cox Sterile Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?