FDA applicant

Surgiquip, Inc.

Tulsa, OK5 decisions1994–19940 recalls

FDA records 5 decisions for Surgiquip, Inc. (Tulsa, OK) in 1994: 5 510(k) clearances. Most are in product codes HWE (Instrument, Surgical, Orthopedic, Ac-Powered…) and GFA (Blade, Saw, General & Plastic Surgery, Surgical). 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 Surgiquip, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgiquip, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Surgiquip, Inc.

Which product codes does it file in?

What has FDA decided for it lately?