FDA applicant

Andrew Surgical

Plymouth, MN1 decision1991–19910 recalls

FDA records 1 decision for Andrew Surgical (Plymouth, MN) in 1991: 1 510(k) clearance. 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 Andrew Surgical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Andrew Surgical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Andrew”

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

Andrew Technologies, LLC 3 Andrew V. Stadler 1 Andrew G. Halpern 1

Andrew Surgical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Andrew”