Rebotix
Rebotix appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 20, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250417 | Remanufactured EndoWrist Cobra Grasper (420190) | Aug 20, 2025 |
| K250399 | Remanufactured EndoWrist Cadiere Forceps (420049) | Aug 19, 2025 |
| K250539 | Remanufactured EndoWrist Tenaculum Forceps (420207) | Aug 19, 2025 |
| K250387 | Remanufactured EndoWrist Long Tip Forceps (420048) | Aug 19, 2025 |
| K241872 | Remanufactured EndoWrist ProGrasp Forceps (420093) | Nov 7, 2024 |