Choicespine, LP
Country not established
- Devices
- 9,815
What Choicespine, LP makes
Choicespine, LP manufactures spinal fusion devices, including polymeric and metallic interbody cages for intervertebral support, non-bioabsorbable bone screws for internal spinal fixation, and spinal fixation plates. Their portfolio also includes non-sterile and sterile polymeric spinal fusion cages, as well as systems for lateral interbody fusion and minimally invasive pedicle screw fixation.
The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 9,815 devicesShowing 1-50 of 9,815
Frequently asked questions
How many devices does Choicespine, LP have in the registry?
The registry currently lists 9815 devices for Choicespine, LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list Choicespine, LP's devices?
Among its 50 most recently registered devices, Choicespine, LP has devices listed in FDA GUDID (50 devices).
What risk classes do Choicespine, LP's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Choicespine, LP's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Choicespine, LP in the registry?
The most recently registered devices listed for Choicespine, LP include BOOMERANG BT20-D4513, BOOMERANG BT20-D4515, Boomerang BT20-D4517 and BOOMERANG B070-0000.