510(k) Report

FDA applicant

Rebstock - Instrumente GmbH

Duerbheim, DE1 decision2001–20010 recalls

FDA records 1 decision for Rebstock - Instrumente GmbH (Duerbheim, DE) in 2001: 1 510(k) clearance. All are in product code HCH (Clip, Aneurysm). 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 Rebstock - Instrumente GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rebstock - Instrumente GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rebstock - 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?

  • HCHClip, Aneurysm1decision

What has FDA decided for it lately?

  • K003500Rebstock Yasargil Aneurysm ClipRebstock - Instrumente GmbH · 2001

The one decision as Rebstock - Instrumente GmbH →