Rebotix
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories1
Latest FDA decision2025-08-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250417 | Remanufactured EndoWrist Cobra Grasper (420190) | QSM | 2025-08-20 | View |
| 510(k) | K250387 | Remanufactured EndoWrist Long Tip Forceps (420048) | QSM | 2025-08-19 | View |
| 510(k) | K250399 | Remanufactured EndoWrist Cadiere Forceps (420049) | QSM | 2025-08-19 | View |
| 510(k) | K250539 | Remanufactured EndoWrist Tenaculum Forceps (420207) | QSM | 2025-08-19 | View |
| 510(k) | K241872 | Remanufactured EndoWrist ProGrasp Forceps (420093) | QSM | 2024-11-07 | View |
No matching devices.