Re Walk Robotics, Ltd.
Country not established
- Devices
- 4
What Re Walk Robotics, Ltd. makes
ReWalk Robotics, Ltd. makes the ReWalk Restore, a powered exoskeleton designed to assist individuals with mobility impairments in walking and standing.
The ReWalk Restore is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
ReWalk P6.0 Ref K221696
Regimes: 510(k) Registry: 510(k)ReWalk P6.0 Ref K200032
Regimes: 510(k) Registry: 510(k)ReWalk(TM) Ref K160987
Regimes: 510(k) Registry: 510(k)ReWalk Restore Ref K190337
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Re Walk Robotics, Ltd. have in the registry?
The registry currently lists 4 devices for Re Walk Robotics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Re Walk Robotics, Ltd.'s devices?
Among its 4 most recently registered devices, Re Walk Robotics, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Re Walk Robotics, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Re Walk Robotics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Re Walk Robotics, Ltd. in the registry?
The most recently registered devices listed for Re Walk Robotics, Ltd. include ReWalk P6.0, ReWalk(TM) and ReWalk Restore.