FDA applicant

International Implant Seminars

Canada, CA4 decisions1995–19950 recalls

FDA records 4 decisions for International Implant Seminars (Canada, CA) in 1995: 4 510(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 International Implant Seminars’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for International Implant Seminars since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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International Implant Seminars

Which product codes does it file in?

What has FDA decided for it lately?