FDA applicant

France Orthodontie

Tours, FR1 decision1995–19950 recalls

FDA records 1 decision for France Orthodontie (Tours, FR) in 1995: 1 510(k) clearance. All are in product code DZB (Headgear, Extraoral, Orthodontic). 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 France Orthodontie’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for France Orthodontie since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “France”

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

France Chirurgae Instrumentation 1

France Orthodontie

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “France”