510(k) Report

FDA applicant

Dr. Ihde Dental AG Switzerland

New York, NY1 decision2001–20010 recalls

FDA records 1 decision for Dr. Ihde Dental AG Switzerland (New York, NY) in 2001: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Dr. Ihde Dental AG Switzerland’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. Ihde Dental AG Switzerland since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. Ihde Dental AG Switzerland by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K991822Allfit Implant System, Short Neck, Model Sti RT Length, Allfit Implant System, Long Neck, Model Sti RT LN…Dr. Ihde Dental AG Switzerland · 2001

The one decision as Dr. Ihde Dental AG Switzerland →