ReWalk? 7 Personal Exoskeleton (50-20-0005)
Mar 2025
261d
Rewalk Robotics Ltd. Dba Lifeward
1
Total
1
Cleared
0
Denied
Rewalk Robotics Ltd. Dba Lifeward — FDA 510(k) Submissions
Rewalk Robotics Ltd. Dba Lifeward has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Powered Exoskeleton . Use the specialty filter in the sidebar to narrow results.
1 devices