EU → North America Device Access

Ovesco Endoscopy AG

DE-MF-000006426 · Germany · Tuebingen

Ovesco Endoscopy AG is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIb5
Class IIa2

Most frequent device types declared: OTSC System Set.

Among these devices, 6 are declared sterile, 5 implantable, 4 active.

Devices declared under this manufacturer

Catalogue references include 100.01, 100.03, 100.51sf, 200.70n, 200.72n, 200.76n.

European nomenclature codes declared: G030299, G030202, V80.

United States market access

FDA establishment registerRegistered with FDA
Matched entryOVESCO ENDOSCOPY AG (DE) · FDA 3006696607
Devices in EUDAMED7
Country of registrationGermany

Device-level evidence

Devices with a numeric GTIN7
Found in the U.S. device database2
Share28.6 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryOVESCO ENDOSCOPY AG

What it holds in Canada

Licences on record8
Currently active0
Class 2 devices6
Class 3 devices2
First licensed2025-11-17

Licence types: Single Device (4), Device Group Family (2), Device Family (2).

Licensed under: COLONIC/DIAGNOSTIC FTRD SET, FTRD PROVE CAP, FTRD GRASPER, OTSG XCAVATOR, OTSC ANCHOR, ARGOCAP.

North American profile: Both markets. Ovesco Endoscopy AG is registered in both the United States and Canada.

Other manufacturers in Germany

All Germany manufacturers →