510(k) Report

FDA applicant

Cl Medical

Sainte Foy Les Lyon, FR2 decisions2005–20060 recalls

FDA records 2 decisions for Cl Medical (Sainte Foy Les Lyon, FR) from 2005 to 2006: 2 510(k) clearances. Most are in product codes OTN (Mesh, Surgical, Synthetic, Urogynecologic, For…) and OTM (Mesh, Surgical, For Stress Urinary…). Its devices cite 8 predicates, 1 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Cl Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cl Medical 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?

  • OTNMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic…1decision
  • OTMMesh, Surgical, For Stress Urinary Incontinence, Male1decision

Whose devices does it build on?

Its devices cite 8 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K051533I-STOPCl Medical · 20051cites it

What has FDA decided for it lately?

  • K063079I-Stop Trans Obturator Male SlingCl Medical · 2006
  • K051533I-STOPCl Medical · 2005

All 2 as Cl Medical →