Medical Device Manufacturer · US , Plymouth , MN

Reprise Biomedical - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Reprise Biomedical has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Reprise Biomedical Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Reprise Biomedical

1 devices

1-1 of 1