510(k) Report

FDA applicant

Von Zeppelin Chirurgische Instrumente GmbH

Germany, DE1 decision1992–19920 recalls

FDA records 1 decision for Von Zeppelin Chirurgische Instrumente GmbH (Germany, DE) in 1992: 1 510(k) clearance. All are in product code HBE (Drills, Burrs, Trephines & Accessories…). 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, neurology panel, where it files most

How often FDA has decided Von Zeppelin Chirurgische Instrumente GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Von Zeppelin Chirurgische Instrumente GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Von Zeppelin Chirurgische Instrumente GmbH 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?

  • HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K922299Zeppelin Motor Drill SystemVon Zeppelin Chirurgische Instrumente GmbH · 19923cite it

What has FDA decided for it lately?

  • K922299Zeppelin Motor Drill SystemVon Zeppelin Chirurgische Instrumente GmbH · 1992

The one decision as Von Zeppelin Chirurgische Instrumente GmbH →