FDA applicant

Comeg Endoscopy

Aurora, CO3 decisions1997–19970 recalls

FDA records 3 decisions for Comeg Endoscopy (Aurora, CO) in 1997: 3 510(k) clearances. Most are in product codes OCX (Endoscopic Irrigation/Suction System) and FJL (Resectoscope). 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 Endoscopy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Comeg Endoscopy since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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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 Endoskopie GmbH 1 Comeg USA, Inc. 1

Comeg Endoscopy

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Comeg”