Cyberdyne, Inc. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Cyberdyne, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Medical HAL Lower Limb Type (HAL-ML), HAL for Medical Use(Lower Limb type)
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) Regulatory Record - Cyberdyne, Inc.
3 devices