Biorez, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biorez, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The BioBrace Implant
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.
FDA 510(k) Regulatory Record - Biorez, Inc.
1 devices