FDA applicant

American Dent-All, Inc.

Glendale, CA5 decisions2000–20030 recalls

FDA records 5 decisions for American Dent-All, Inc. (Glendale, CA) from 2000 to 2003: 5 510(k) clearances. All are in product code EJH (Alloy, Metal, Base). 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 American Dent-All, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Dent-All, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Dent-All, Inc.

Which product codes does it file in?

What has FDA decided for it lately?