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Sign in to claim this brandOSSIO LTD
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- ossio.io
- —
- —
- [email protected]
- Phone
- 1-833-781-7373
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 600505107
Catalogue (110)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| OSSIOfiber® Threaded Trimmable Fixation Nail | K241277 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Interference Screw | K252022 | FDA 510(k) | Class II | Active |
| OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation Nail, Cannulated Design | K203465 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Threaded Trimmable Fixation Nails | K233198 | FDA 510(k) | Class II | Active |
| OSSIOfiber Suture Anchor | K213415 | FDA 510(k) | Class II | Active |
| OSSIO™ Pin Product Family | K181180 | FDA 510(k) | Class II | Active |
| OSSIOfiber Compression Screw, 3.5mm | K213596 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Staple | K212594 | FDA 510(k) | Class II | Active |
| OSSIOfiber Compression Screw, OSSIOfiber Compression Screw, 6.5mm | K221193 | FDA 510(k) | Class II | Active |
| OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation Implant | K201803 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Ossio Ltd. Caesarea Central · IL FEI 3014554088