510(k) Report

FDA applicant

Team Mfg., Inc.

Augusta, GA3 decisions1991–19920 recalls

FDA records 3 decisions for Team Mfg., Inc. (Augusta, GA) from 1991 to 1992: 3 510(k) clearances. Most are in product codes IPQ (Unnamed device) and EFQ (Gauze/Sponge, Internal). 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 Team Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Team Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Team 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 “Team”

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