FDA applicant

Rudolf Storz GmbH

Amsterdam, NL1 decision2004–20040 recalls

FDA records 1 decision for Rudolf Storz GmbH (Amsterdam, NL) in 2004: 1 510(k) clearance. All are in product code HBO (Clip, Scalp). 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 Rudolf Storz GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rudolf Storz GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Rudolf”

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

Rudolf Riester GmbH & Co. KG 33 Rudolf Medical GmbH + Co. KG 1

Rudolf Storz GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rudolf”