Company ยท US
Rebotix
FDA 510(k) clearances and medical device recalls filed under this name, 2024 to 2025. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| QSM | System, Surgical, Computer Controlled Instrument, Remanufactured | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 20, 2025 | K250417 | Remanufactured EndoWrist Cobra Grasper (420190) Rebotix | QSM |
| Aug 19, 2025 | K250539 | Remanufactured EndoWrist Tenaculum Forceps (420207) Rebotix | QSM |
| Aug 19, 2025 | K250399 | Remanufactured EndoWrist Cadiere Forceps (420049) Rebotix | QSM |
| Aug 19, 2025 | K250387 | Remanufactured EndoWrist Long Tip Forceps (420048) Rebotix | QSM |
| Nov 7, 2024 | K241872 | Remanufactured EndoWrist ProGrasp Forceps (420093) Rebotix | QSM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||