FDA applicant

Altatec Biotechnologies

Potomac, MD4 decisions2000–20030 recalls

FDA records 4 decisions for Altatec Biotechnologies (Potomac, MD) from 2000 to 2003: 4 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NHA (Abutment, Implant, Dental, Endosseous). 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 Altatec Biotechnologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Altatec Biotechnologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Altatec”

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

Altatec GmbH 14 Altatec Biotechnologies N.A., Inc. 1

Altatec Biotechnologies

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?

Other applicant names beginning “Altatec”