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Cyberdyne, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233695Medical HAL Lower Limb Type (HAL-ML)May 7, 2024
K201559HAL for Medical Use(Lower Limb type)October 2, 2020
K171909HAL for Medical Use (Lower Limb Type)December 17, 2017