FDA applicant

Dixon Medical, Inc.

Atlanta, GA12 decisions1990–19900 recalls

FDA records 12 decisions for Dixon Medical, Inc. (Atlanta, GA) in 1990: 12 510(k) clearances. All are in product code HET (Laparoscope, Gynecologic (And Accessories)). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Dixon Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dixon Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?