FDA applicant

Compagnie Oris Industrie, S.A.

France, FR2 decisions1986–19890 recalls

FDA records 2 decisions for Compagnie Oris Industrie, S.A. (France, FR) from 1986 to 1989: 2 510(k) clearances. Most are in product codes JAQ (System, Applicator, Radionuclide…) and CKG (Radioimmunoassay, Acth). 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 Compagnie Oris Industrie, S.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Compagnie Oris Industrie, S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Compagnie”

FDA records each applicant name separately; these may or may not be the same firm.

Compagnie Financiere & Medicale (Cf&M) 1 Compagnie DE Developpement Aguettant 1

Compagnie Oris Industrie, S.A.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Compagnie”