FDA applicant

Southwest Medical Mfg., Inc.

Marietta, GA2 decisions1990–19920 recalls

FDA records 2 decisions for Southwest Medical Mfg., Inc. (Marietta, GA) from 1990 to 1992: 2 510(k) clearances. Most are in product codes HFB (Forceps, Biopsy, Gynecological) and GCJ (Laparoscope, General & Plastic Surgery). 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 Southwest Medical Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Southwest Medical Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Southwest”

FDA records each applicant name separately; these may or may not be the same firm.

Southwest Technologies, Inc. 5 Southwest Artificial Eyes, Inc. 2 Southwest Ergonomics 1

Southwest Medical Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Southwest”