Medical Device Manufacturer · US , Plymouth , MN

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

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Activortho, Inc. has 2 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Activortho, Inc.

2 devices

1-2 of 2