Rewalk Robotics Ltd. Dba Lifeward - FDA 510(k) Cleared Devices
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) cleared devices by Rewalk Robotics Ltd. Dba Lifeward
1 devices