510(k) Report

FDA applicant

United American Medical Co., Inc.

Mc Minnville, TN3 decisions1991–19940 recalls

FDA records 3 decisions for United American Medical Co., Inc. (Mc Minnville, TN) from 1991 to 1994: 3 510(k) clearances. All are in product code HWE (Instrument, Surgical, Orthopedic, Ac-Powered…). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for United American Medical Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like United American Medical Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report