FDA applicant

Pacific Implant, Inc.

Walker, MI2 decisions1981–19990 recalls

FDA records 2 decisions for Pacific Implant, Inc. (Walker, MI) from 1981 to 1999: 2 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EKL (Point, Silver, Endodontic). 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 Pacific Implant, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pacific Implant, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pacific Implant, Inc.

Which product codes does it file in?

What has FDA decided for it lately?