Neogenix, LLC Dba Ogenix

Neogenix, LLC Dba Ogenix — FDA 510(k) Submissions

Neogenix, LLC Dba Ogenix has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Chamber, Oxygen, Topical, Extremity . Use the specialty filter in the sidebar to narrow results.