Rebotix
Country not established
- Devices
- 5
What Rebotix makes
Rebotix specializes in remanufactured laparoscopic surgical instruments, including EndoWrist Cobra Graspers, Long Tip Forceps, Cadiere Forceps, ProGrasp Forceps, and Tenaculum Forceps. These devices are designed for minimally invasive procedures, offering precision gripping and cutting functions for abdominal and thoracic surgeries.
The company’s portfolio consists of Class II devices, all of which are listed via the FDA’s 510(k) pathway. These instruments are regulated under U.S. medical device laws and are intended for use in laparoscopic surgery. Rebotix operates from the United States.
Catalogue
Remanufactured EndoWrist Cobra Grasper (420190) Ref K250417
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rebotix have in the registry?
The registry currently lists 5 devices for Rebotix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rebotix's devices?
Among its 5 most recently registered devices, Rebotix has devices listed in FDA 510(k) (5 devices).
What risk classes do Rebotix's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Rebotix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rebotix in the registry?
The most recently registered devices listed for Rebotix include Remanufactured EndoWrist Cobra Grasper (420190), Remanufactured EndoWrist Long Tip Forceps (420048), Remanufactured EndoWrist Cadiere Forceps (420049) and Remanufactured EndoWrist ProGrasp Forceps (420093).