FDA applicant

Kodak-Trophy

Marne La Vallee Cedex 2, FR1 decision2006–20062 recalls

FDA records 1 decision for Kodak-Trophy (Marne La Vallee Cedex 2, FR) in 2006: 1 510(k) clearance. All are in product code EHD (Unit, X-Ray, Extraoral With Timer). 2 recalls are 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 Kodak-Trophy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kodak-Trophy since 2007.

Recalls per year

2in 2014

2007high 2 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Kodak-Trophy”

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

Kodak Health Imaging Systems, Inc. 6 Kodak Clinical Diagnostics, Ltd. 1

Kodak-Trophy

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Kodak-Trophy”