510(k) Report

FDA applicant

Medicamat S.A.

Washington, DC2 decisions1995–19970 recalls

FDA records 2 decisions for Medicamat S.A. (Washington, DC) from 1995 to 1997: 2 510(k) clearances. Most are in product codes LFL (Instrument, Ultrasonic Surgical) and GAH (Stylet, Surgical, General & Plastic Surgery). 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 Medicamat S.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medicamat S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medicamat S.A. 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?

  • LFLInstrument, Ultrasonic Surgical1decision
  • GAHStylet, Surgical, General & Plastic Surgery1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K952737Calvitron Hair Transplant SystemMedicamat S.A. · 19951cites it

What has FDA decided for it lately?

  • K972148B.U.S. EndotronMedicamat S.A. · 1997
  • K952737Calvitron Hair Transplant SystemMedicamat S.A. · 1995

All 2 as Medicamat S.A. →