Rewalk Robotics Ltd. Dba Lifeward
IsraelFDA applicant, unverified
- Devices
- 1
What Rewalk Robotics Ltd. Dba Lifeward makes
Lifeward manufactures the ReWalk 7 Personal Exoskeleton, which is a wearable robotic device designed to assist individuals with mobility impairments.
The company is based in the United States, and its device is classified as Class II and listed within the FDA 510(k) regulatory registry.
Catalogue
ReWalk® 7 Personal Exoskeleton (50-20-0005) Ref K241822
Regimes: CE MDR 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rewalk Robotics Ltd. Dba Lifeward have in the registry?
The registry currently lists 1 device for Rewalk Robotics Ltd. Dba Lifeward. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rewalk Robotics Ltd. Dba Lifeward's devices?
Among its 1 most recently registered device, Rewalk Robotics Ltd. Dba Lifeward has devices listed in FDA 510(k) (1 device).
What risk classes do Rewalk Robotics Ltd. Dba Lifeward's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rewalk Robotics Ltd. Dba Lifeward's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rewalk Robotics Ltd. Dba Lifeward in the registry?
The most recently registered devices listed for Rewalk Robotics Ltd. Dba Lifeward include ReWalk® 7 Personal Exoskeleton (50-20-0005).