Reprise Biomedical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reprise Biomedical - FDA 510(k) Cleared Devices
Recent clearances: Miro3D Wound Matrix
1
Total
1
Cleared
0
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.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Reprise Biomedical
1 devices