FDA applicant

Forestadent

Germany, DE2 decisions1993–19940 recalls

FDA records 2 decisions for Forestadent (Germany, DE) from 1993 to 1994: 2 510(k) clearances. Most are in product codes EJF (Bracket, Metal, Orthodontic) and DYJ (Retainer, Screw Expansion, 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 Forestadent’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Forestadent since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Forestadent”

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

Forestadent Bernhard Forster GmbH 4

Forestadent

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Forestadent”