Cyberdyne, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Cyberdyne, Inc. has 3 FDA 510(k) cleared medical devices. Based in Tsukuba, JP.
Latest FDA clearance: May 2024. Active since 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cyberdyne, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cyberdyne, Inc.
3 devices