FDA applicant

Sims Surgical, Inc.

Keene, NH3 decisions1990–19903 recalls

FDA records 3 decisions for Sims Surgical, Inc. (Keene, NH) in 1990: 3 510(k) clearances. Most are in product codes BSR (Stylet, Tracheal Tube) and GZT (Retractor, Self-Retaining, For Neurosurgery). 3 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Sims Surgical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sims Surgical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sims Surgical, 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

Other applicant names beginning “Sims”

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

Sims Deltec, Inc. 32 Sims Portex, Inc. 16 Sims Level 1, Inc. 2 Sims 2

Sims Surgical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Sims”