510(k) Report

FDA applicant

Lamidey Noury Medical

Verriere Le Buisson, FR2 decisions2022–20240 recalls

FDA records 2 decisions for Lamidey Noury Medical (Verriere Le Buisson, FR) from 2022 to 2024: 2 510(k) clearances. Most are in product codes KNS (Unit, Electrosurgical, Endoscopic (With Or…) and FAS (Electrode, Electrosurgical, Active, Urological). Its devices cite 2 predicates, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Lamidey Noury Medical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2022: 12024: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Lamidey Noury Medical by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)1decision
  • FASElectrode, Electrosurgical, Active, Urological1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K240504PLASMA EDGE SystemLamidey Noury Medical · 2024
  • K222542MCB UNIT Model: V10GMCBUSLamidey Noury Medical · 2022

All 2 as Lamidey Noury Medical →