Ovesco Endoscopy AG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000006426 FEI 3006696607
Ovesco Endoscopy AG is a medical device manufacturer based in Germany, with 125 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class IIb and I) as of 14 Nov 2026.
- Devices
- 125
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 76
- EUDAMED 70
- FDA 510(k) 16
- Device classes
- FDA Class II 81
- EU Class IIb 24
- FDA Class I 11
- EU Class I 9
- Top EMDN categories
- Identifiers
- EUDAMED SRN DE-MF-000006426
- FDA FEI 3006696607
- DUNS 344007369
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
What Ovesco Endoscopy AG makes
Ovesco Endoscopy AG manufactures reusable and single-use devices for gastrointestinal endoscopy, including non-bioabsorbable clips for long-term tissue closure, flexible forceps for tissue manipulation, and monopolar electrosurgical handpieces for controlled tissue resection or biopsy. Their portfolio also includes dilators for treating gastrointestinal stenosis, endoscope channel support kits, and caps for tissue removal or biopsy/resection procedures. Notable examples include the OTSC Anchor system for controlled tissue closure, electrosurgical dissection tools like the Coag Dissector, and the BougieCap for dilation assistance.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. While specific regulatory pathways vary by product, all devices comply with applicable U.S. medical device regulations.
Catalogue
Search and filter all 125 devicesShowing 1-50 of 125
Company details
- EUDAMED SRN
- DE-MF-000006426
- FDA FEI number
- 3006696607
- DUNS number
- 344007369
- EU VAT number
- DE217051960
- EUDAMED status
- Active
- EUDAMED registered name
- Ovesco Endoscopy AG
- EUDAMED abbreviated name
- Ovesco
- Registered address
- 9, Friedrich-Miescher-Strasse, 72076, Tuebingen, Germany
- Website
- www.ovesco.com
- Phone
- +49707196528160
- PRRC contact
- Katrin Steinbrecher
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 16 Nov 2030
DQS Medizinprodukte GmbH 0297 1 certificate
- 1000317372 Active
Quality management system EU MDR
- Issued
- 25 Sep 2026
- Expires
- 16 Nov 2030
- Reason
- Change approved
Frequently asked questions
How many devices does Ovesco Endoscopy AG have in the registry?
The registry currently lists 125 devices for Ovesco Endoscopy AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ovesco Endoscopy AG's devices?
Among its 50 most recently registered devices, Ovesco Endoscopy AG has devices listed in EUDAMED (41 devices), FDA 510(k) (2 devices) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ovesco Endoscopy AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Ovesco Endoscopy AG's devices are Class I, Class IIb and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Ovesco Endoscopy AG?
EUDAMED lists 1 certificate for Ovesco Endoscopy AG (quality management system) under MDR. The most recent was issued on 25 Sep 2026.
What are the newest devices from Ovesco Endoscopy AG in the registry?
The most recently registered devices listed for Ovesco Endoscopy AG include OTSCneo System Set: 12/6 t, ArgoCap, OTSCneo System Set: 14/3 t and OTSCneo System Set: 12/6 gc.