FDA applicant

Trophy Radiologie

Vincennes, Cedex (Paris), FR16 decisions1985–20040 recalls

FDA records 16 decisions for Trophy Radiologie (Vincennes, Cedex (Paris), FR) from 1985 to 2004: 16 510(k) clearances. Most are in product codes EHD (Unit, X-Ray, Extraoral With Timer) and EIA (Unit, Operative Dental). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Trophy Radiologie since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Trophy Radiologie’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Trophy”

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

Trophy 15 Trophy Skin, Inc. 3

Trophy Radiologie

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?

Other applicant names beginning “Trophy”