Ht Medical, LLC
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
NeoFuse HA Enhanced PLIF/TLIF Ref K170511
Regimes: 510(k) Registry: 510(k)NeoFuse Ti3D PLIF/TLIF/Cervical Interbody Ref K170318
Regimes: 510(k) Registry: 510(k)NeoFuse HA Enhanced PLIF/TLIF Ref K153615
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ht Medical, LLC have in the registry?
The registry currently lists 3 devices for Ht Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ht Medical, LLC's devices?
Among its 3 most recently registered devices, Ht Medical, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Ht Medical, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ht Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ht Medical, LLC in the registry?
The most recently registered devices listed for Ht Medical, LLC include NeoFuse HA Enhanced PLIF/TLIF and NeoFuse Ti3D PLIF/TLIF/Cervical Interbody.