FDA applicant

Minimatic Implant Technology

Deerfield Beach, FL34 decisions1990–19920 recalls

FDA records 34 decisions for Minimatic Implant Technology (Deerfield Beach, FL) from 1990 to 1992: 34 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Minimatic Implant Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minimatic Implant Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Minimatic”

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

Minimatic, Inc. 1

Minimatic Implant Technology

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 “Minimatic”