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Cyberdyne, Inc.

FDA Regulatory Profile

Cyberdyne, Inc. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
May 7, 2024

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

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

FDA data resources