Neogenix, LLC Dba Ogenix
Country not established
- Devices
- 1
What Neogenix, LLC Dba Ogenix makes
Neogenix, LLC (dba Ogenix) manufactures the EPIFLO-28, a medical device designed for the collection, processing, and storage of epithelial cells, intended for use in epithelial cell transplantation procedures.
The EPIFLO-28 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Epiflo-28 Ref K190742
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neogenix, LLC Dba Ogenix have in the registry?
The registry currently lists 1 device for Neogenix, LLC Dba Ogenix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neogenix, LLC Dba Ogenix's devices?
Among its 1 most recently registered device, Neogenix, LLC Dba Ogenix has devices listed in FDA 510(k) (1 device).
What risk classes do Neogenix, LLC Dba Ogenix's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neogenix, LLC Dba Ogenix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neogenix, LLC Dba Ogenix in the registry?
The most recently registered devices listed for Neogenix, LLC Dba Ogenix include EPIFLO-28.