FDA applicant

Dabi-Atlante America Corp.

Tampa, FL4 decisions1991–19940 recalls

FDA records 4 decisions for Dabi-Atlante America Corp. (Tampa, FL) from 1991 to 1994: 4 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EAZ (Light, Operating, 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 Dabi-Atlante America Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dabi-Atlante America Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dabi-Atlante America Corp.

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?