Medical Device Manufacturer · US , Tanner , AL

Curiteva, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

Curiteva, LLC has 4 FDA 510(k) cleared medical devices. Based in Tanner, US.

Historical record: 4 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Curiteva, LLC

4 devices

1-4 of 4