Neurostructures, Inc
United StatesFDA applicant, unverified
- Devices
- 718
What Neurostructures, Inc makes
NeuroStructures, Inc. manufactures orthopaedic and spinal fixation devices, including non-bioabsorbable spinal plates, polymeric interbody fusion cages, and internal fixation systems with screws and plates. Their portfolio also includes reusable positioning instruments for orthopaedic prosthesis implantation and non-sterile bone-screw fixation systems for spinal stabilization.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. NeuroStructures, Inc. is based in the United States.
Catalogue
Search and filter all 718 devicesShowing 1-50 of 718
Company details
- DUNS number
- 079391677
- [email protected]
- Phone
- 8003526103
Frequently asked questions
How many devices does NEUROSTRUCTURES, INC have in the registry?
The registry currently lists 718 devices for NEUROSTRUCTURES, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEUROSTRUCTURES, INC's devices?
Among its 50 most recently registered devices, NEUROSTRUCTURES, INC has devices listed in FDA GUDID (50 devices).
What risk classes do NEUROSTRUCTURES, INC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for NEUROSTRUCTURES, INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NEUROSTRUCTURES, INC in the registry?
The most recently registered devices listed for NEUROSTRUCTURES, INC include Palladian™ 50-06-4525, Cavetto 100018-16188, Cortina 100198-200909 and Cavetto 100018-14164.