Orthogen, LLC
Also registered as Orthogen Corp.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Surgiplaster Calcium Sulfate Hemihydrate Ref K011403
Regimes: 510(k) Registry: 510(k)Nanogen Ref K102208
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthogen, LLC have in the registry?
The registry currently lists 2 devices for Orthogen, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthogen, LLC's devices?
Among its 2 most recently registered devices, Orthogen, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Orthogen, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Orthogen, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthogen, LLC in the registry?
The most recently registered devices listed for Orthogen, LLC include SURGIPLASTER CALCIUM SULFATE HEMIHYDRATE and NANOGEN.