FDA applicant

Smith & Nephew Equipment Group

St. Louis, MO2 decisions1991–19910 recalls

FDA records 2 decisions for Smith & Nephew Equipment Group (St. Louis, MO) in 1991: 2 510(k) clearances. Most are in product codes FSY (Light, Surgical, Ceiling Mounted) and BWN (Table And Attachments, Operating-Room). 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 Smith & Nephew Equipment Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Smith & Nephew Equipment Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Smith & Nephew Equipment Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Smith & Nephew Equipment Group’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

Other applicant names beginning “Smith”

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

Smith & Nephew, Inc. 556 Smith & Nephew Richards, Inc. 88 Smith & Nephew United, Inc. 34 Smith & Nephew Medical Limited 33 Smith & Nephew Dyonics, Inc. 22 Smith & Nephew Endoscopy, Inc. 18 Smith and Nephew Donjoy, Inc. 15 Smith River Biologicals 12 Smith & Nephew, Inc., Orthopaedic Div. 10 Smith & Nephew Perry 10 Smith & Nephew Inc., Endoscopy Div. 10 Smith & Nephew, Mpl Division 9

Smith & Nephew Equipment Group

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Smith”