FDA applicant

Arplay Medical S.A.

Izeure, Cote D'Or, FR9 decisions2001–20020 recalls

FDA records 9 decisions for Arplay Medical S.A. (Izeure, Cote D'Or, FR) from 2001 to 2002: 9 510(k) clearances. Most are in product codes IYE (Accelerator, Linear, Medical) and IXI (Block, Beam-Shaping, Radiation Therapy). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Arplay Medical S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arplay Medical S.A. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Arplay Medical S.A.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?