Medical Device Manufacturer · US , Plymouth , MN

Reprise Biomedical, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2022

Total

Cleared

Denied

Reprise Biomedical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Latest FDA clearance: Apr 2024. Active since 2022. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Reprise Biomedical, Inc.

4 devices

1-4 of 4