FDA applicant

Angiomed GmbH & Co. Medizintechnik KG

Germany, DE1 decision1992–19920 recalls

FDA records 1 decision for Angiomed GmbH & Co. Medizintechnik KG (Germany, DE) in 1992: 1 510(k) clearance. All are in product code KNW (Instrument, Biopsy). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Angiomed GmbH & Co. Medizintechnik KG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Angiomed GmbH & Co. Medizintechnik KG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Angiomed GmbH & Co. Medizintechnik KG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Angiomed GmbH & Co. Medizintechnik KG’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Angiomed”

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

Angiomed U.S., Inc. 24

Angiomed GmbH & Co. Medizintechnik KG

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Angiomed”