Biogennix is one of 20245 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biogennix - FDA 510(k) Cleared Devices
Recent clearances: osteoSPAN Morpheus
1
Total
1
Cleared
0
Denied
Biogennix has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biogennix Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biogennix
1 devices