# Rebotix

- Location (FDA's records): St. Petersburg, FL
- FDA decisions: 5 (2024–2025): 5 510(k) clearances
- Product codes: QSM (5)
- 510(k) review time since 2016: median 188 days, against 188 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 15 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Intuitive Surgical, Inc.: 15 (https://510kreport.com/company/intuitive-surgical)

## Recent decisions
- K250417: Remanufactured EndoWrist Cobra Grasper (420190) (Aug 20, 2025)
- K250539: Remanufactured EndoWrist Tenaculum Forceps (420207) (Aug 19, 2025)
- K250387: Remanufactured EndoWrist Long Tip Forceps (420048) (Aug 19, 2025)
- K250399: Remanufactured EndoWrist Cadiere Forceps (420049) (Aug 19, 2025)
- K241872: Remanufactured EndoWrist ProGrasp Forceps (420093) (Nov 7, 2024)

Source page: https://510kreport.com/company/rebotix