FDA applicant

Comeg Endoskopie GmbH

Aurora, CO1 decision1997–19970 recalls

FDA records 1 decision for Comeg Endoskopie GmbH (Aurora, CO) in 1997: 1 510(k) clearance. All are in product code OCZ (Endoscopic Grasping/Cutting Instrument…). 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 Comeg Endoskopie GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Comeg Endoskopie GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Comeg Endoskopie 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 “Comeg”

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

Comeg Endoscopy 3 Comeg USA, Inc. 1

Comeg Endoskopie GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Comeg”