Ht Medical, LLC is one of 18422 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ht Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: NeoFuse Ti3D PLIF/TLIF/Cervical Interbody, NeoFuse HA Enhanced PLIF/TLIF, NeoFuse HA Enhanced PLIF/TLIF
3
Total
3
Cleared
0
Denied
Ht Medical, LLC has 3 FDA 510(k) cleared medical devices. Based in Tulsa, US.
Historical record: 3 cleared submissions from 2016 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ht Medical, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Additive Innovations, LLC and Acknowledge Regulatory Strategies, LLC.
FDA 510(k) Regulatory Record - Ht Medical, LLC
3 devices