FDA applicant

Bernsco Surgical Supply, Inc.

Seattle, WA4 decisions1988–19920 recalls

FDA records 4 decisions for Bernsco Surgical Supply, Inc. (Seattle, WA) from 1988 to 1992: 4 510(k) clearances. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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 Bernsco Surgical Supply, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bernsco Surgical Supply, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bernsco Surgical Supply, 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

Bernsco Surgical Supply, Inc.

Which product codes does it file in?

What has FDA decided for it lately?