Biorez, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biorez, Inc. has 1 FDA 510(k) cleared medical devices. Based in New Haven, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biorez, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
1 devices