Rewalk Robotics Ltd. Dba Lifeward is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Rewalk Robotics Ltd. Dba Lifeward - FDA 510(k) Cleared Devices
Recent clearances: ReWalk® 7 Personal Exoskeleton (50-20-0005)
1
Total
1
Cleared
0
Denied
Rewalk Robotics Ltd. Dba Lifeward has 1 FDA 510(k) cleared medical devices. Based in Yokneam Ilit, IL.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Rewalk Robotics Ltd. Dba Lifeward Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rewalk Robotics Ltd. Dba Lifeward
1 devices