Re Walk Robotics , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Re Walk Robotics , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ReWalk P6.0, ReWalk P6.0, ReWalk Restore
3
Total
3
Cleared
0
Denied
Re Walk Robotics , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Yokneam, IL.
Last cleared in 2023. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Re Walk Robotics , Ltd. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Re Walk Robotics , Ltd.
3 devices