510(k) Report

FDA applicant

Instruments Medicaux G.B., Inc.

Sherbrooke, Quebec, CA2 decisions2001–20020 recalls

FDA records 2 decisions for Instruments Medicaux G.B., Inc. (Sherbrooke, Quebec, CA) from 2001 to 2002: 2 510(k) clearances. Most are in product codes KNF (Coagulator-Cutter, Endoscopic, Unipolar (And…) and GCJ (Laparoscope, General & Plastic Surgery). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Instruments Medicaux G.B., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Instruments Medicaux G.B., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KNFCoagulator-Cutter, Endoscopic, Unipolar (And Accessories)1decision
  • GCJLaparoscope, General & Plastic Surgery1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K022979Laparette, Model Lap J L S H NInstruments Medicaux G.B., Inc. · 2002
  • K010220Xtractor, Model M143Instruments Medicaux G.B., Inc. · 2001

All 2 as Instruments Medicaux G.B., Inc. →