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.

Curiteva, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Curiteva, LLC

4 devices

1-4 of 4