Genprime, Inc. is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genprime, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GenPrime Snap-Top Split Key Cup, GENPRIME DRUGS OF ABUSE READER SYSTEM
2
Total
2
Cleared
0
Denied
Genprime, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oms River, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Genprime, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Newworld Regulatory Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Genprime, Inc.
2 devices