FDA applicant

Thompson Surgical Instruments, Inc.

Traverse City, MI3 decisions2008–20220 recalls

FDA records 3 decisions for Thompson Surgical Instruments, Inc. (Traverse City, MI) from 2008 to 2022: 3 510(k) clearances. Most are in product codes GZT (Retractor, Self-Retaining, For Neurosurgery) and FST (Light, Surgical, Fiberoptic). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Thompson Surgical Instruments”.

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

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

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

FDA decisions per year

1in 2022

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Thompson Surgical Instruments, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Thompson Surgical Instruments, 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 “Thompson”

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

Thompson Respiration Products, Inc. 6 Thompson Mis, Inc. 1

Thompson Surgical Instruments, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Thompson”