# Ht Medical, LLC

- Location (FDA's records): Tulsa, OK
- FDA decisions: 3 (2016–2017): 3 510(k) clearances
- Product codes: MAX (2), ODP (1)
- 510(k) review time since 2016: median 141 days, against 116 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Meditech Spine, LLC: 1 (https://510kreport.com/company/meditech-spine)
- Spinefrontier, Inc.: 1 (https://510kreport.com/company/spinefrontier)
- Cutting Edge Spine, LLC: 1 (https://510kreport.com/company/cutting-edge-spine)
- K2m, Inc.: 1 (https://510kreport.com/company/k2m)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Kalitec Direct, LLC: 1 (https://510kreport.com/company/kalitec-direct)
- Ht Medical D.B.A. Xenix Medical: 1 (https://510kreport.com/company/ht-medical-dba-xenix-medical)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Bespoke Technologies, LLC: 1 (https://510kreport.com/company/bespoke-technologies)
- Kalitec Medical, LLC: 1 (https://510kreport.com/company/kalitec-medical)

## Its most-cited devices
- K170318: NeoFuse Ti3D PLIF/TLIF/Cervical Interbody (2017), cited by 5
- K153615: NeoFuse HA Enhanced PLIF/TLIF (2016), cited by 1

## Recent decisions
- K170318: NeoFuse Ti3D PLIF/TLIF/Cervical Interbody (Jul 12, 2017)
- K170511: NeoFuse HA Enhanced PLIF/TLIF (Apr 25, 2017)
- K153615: NeoFuse HA Enhanced PLIF/TLIF (May 6, 2016)

Source page: https://510kreport.com/company/ht-medical