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Germany·DE-MF-000006426
Last updated September 17, 2026
Information
- Country
- Germany
- Address
- 9, Friedrich-Miescher-Strasse, Tuebingen, Germany
- Website
- www.ovesco.com
- —
- —
- [email protected]
- Phone
- +49707196528160
- PRRC Contact
- Katrin Steinbrecher
- EUDAMED SRN
- DE-MF-000006426
- FDA FEI Number
- 3006696607
- DUNS Number
- —
Catalogue (15)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| stentfix OTSC System Set | K183309 | FDA 510(k) | Class II | Active |
| gastroduodenal FTRD Set | K200684 | FDA 510(k) | Class II | Active |
| Traction Polypectomy Snare | K140923 | FDA 510(k) | Class II | Active |
| Otsc (over-The Scope-Clip) System Set | K101428 | FDA 510(k) | Class II | Active |
| OTSCneo System Set (100.03n-14n, 100.27n-31n) | K251562 | FDA 510(k) | Class II | Active |
| remOVE System | DEN160014 | FDA 510(k) | Class II | Active |
| Aqanife | K141790 | FDA 510(k) | Class II | Active |
| BARS Set (100.60) | K241858 | FDA 510(k) | Class II | Active |
| OTSC Proctology | K150067 | FDA 510(k) | Class II | Active |
| Endo-Maryland Dissector | K141794 | FDA 510(k) | Class II | Active |
| FTRD System Set | K153550 | FDA 510(k) | Class II | Active |
| ArgoCap (200.52) | K242586 | FDA 510(k) | Class II | Active |
| FTRD System Set | K170867 | FDA 510(k) | Class II | Active |
| LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02) | K221385 | FDA 510(k) | Class II | Active |
| remOVE Footswitch | 400.06 | EUDAMED | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Ovesco Endoscopy AG US