Hd Lifesciences, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Hd Lifesciences, LLC makes
Hd Lifesciences, LLC manufactures spinal interbody fusion systems, including standalone anterior lumbar implants, cervical interbody devices for lateral approaches, and lumbar interbody systems designed for posterior or lateral placement.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
HD LifeSciences Cervical IBFD System Ref K180364
Regimes: 510(k) Registry: 510(k)HD Lumbar Interbody System Ref K170676
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hd Lifesciences, LLC have in the registry?
The registry currently lists 3 devices for Hd Lifesciences, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hd Lifesciences, LLC's devices?
Among its 3 most recently registered devices, Hd Lifesciences, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Hd Lifesciences, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Hd Lifesciences, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hd Lifesciences, LLC in the registry?
The most recently registered devices listed for Hd Lifesciences, LLC include Hive™ Stand-alone Anterior Lumbar Interbody System, HD LifeSciences Cervical IBFD System and HD Lumbar Interbody System.