Rebotix

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250417Remanufactured EndoWrist Cobra Grasper (420190)August 20, 2025
K250399Remanufactured EndoWrist Cadiere Forceps (420049)August 19, 2025
K250387Remanufactured EndoWrist Long Tip Forceps (420048)August 19, 2025
K250539Remanufactured EndoWrist Tenaculum Forceps (420207)August 19, 2025
K241872Remanufactured EndoWrist ProGrasp Forceps (420093)November 7, 2024