Medical Device Manufacturer · US , Irvine , CA

Medynus, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2021
3
Total
3
Cleared
0
Denied

Medynus, Inc. has 3 FDA 510(k) cleared medical devices. Based in Irvine, US.

Last cleared in 2022. Active since 2021. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Medynus, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Eerkie Corporation as regulatory consultant.

FDA 510(k) Regulatory Record - Medynus, Inc.
3 devices
1-3 of 3
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All3 Orthopedic 3