Medical Device Manufacturer · DE , Karlsruhe

Ovesco Endoscopy AG - FDA 510(k) Cleared Devices

14 submissions · 13 cleared · Since 2010

Total

Cleared

Denied

FDA 510(k) Regulatory Record - Ovesco Endoscopy AG General & Plastic Surgery ✕

1 devices

1-1 of 1

PCCP authorized FDA software change control pathway

Regulatory consultant 510(k) submission support ecosystem

Novineon CRO GmbH

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026