Nu Vasive, Incorporated
United StatesFDA applicant, unverified
- Devices
- 112
What Nu Vasive, Incorporated makes
Nu Vasive, Incorporated manufactures spinal fixation hardware, including metallic interbody fusion cages for lumbar and anterior lumbar interbody fusion (ALIF) procedures, expandable lateral lumbar interbody systems, and screw-based internal fixation connectors for spinal stabilization. Trial implants for spinal procedures are also part of the portfolio, alongside systems for posterior and transforaminal lumbar interbody fusion (TLIF). The company produces titanium-based and modular fixation solutions designed for surgical spinal reconstruction and stabilization.
The company’s devices are classified as Class II under FDA regulations and are authorised via the 510(k) and Unique Device Identification (UDI) pathways. Products are listed in the FDA’s 510(k) and UDI registries, reflecting compliance with US medical device regulations. Nu Vasive, Incorporated is headquartered in the United States.
Catalogue
Search and filter all 112 devicesShowing 1-50 of 112
Frequently asked questions
How many devices does Nu Vasive, Incorporated have in the registry?
The registry currently lists 112 devices for Nu Vasive, Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nu Vasive, Incorporated's devices?
Among its 50 most recently registered devices, Nu Vasive, Incorporated has devices listed in FDA 510(k) (50 devices).
What risk classes do Nu Vasive, Incorporated's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Nu Vasive, Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nu Vasive, Incorporated in the registry?
The most recently registered devices listed for Nu Vasive, Incorporated include NuVasive 3DP Interfixated ALIF System, NUVASIVE NVM5 SYSTEM, CoRoent® Ti-C System and NuVasive® VersaTie System.