Neogenix, LLC Dba Ogenix - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neogenix, LLC Dba Ogenix has 1 FDA 510(k) cleared medical devices. Based in Beachwood, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neogenix, LLC Dba Ogenix Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Neogenix, LLC Dba Ogenix
1 devices