Neogenix, LLC Dba Ogenix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neogenix, LLC Dba Ogenix - FDA 510(k) Cleared Devices
Recent clearances: EPIFLO-28
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Neogenix, LLC Dba Ogenix
1 devices