Evolution Spine, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3012428435
- Devices
- 3,478
- Registrations
- FDA
- FDA recalls
- 0
What Evolution Spine, LLC makes
Evolution Spine, LLC manufactures metallic and polymeric spinal interbody fusion cages, non-bioabsorbable spinal bone screws, and internal spinal fixation rods. The company also produces spinal fixation plates, spinal implant trials, reusable instrument trays, and orthopaedic inorganic implant inserters and extractors.
The company is based in the United States, and its portfolio consists of Class I and Class II medical devices. These products are listed in the FDA UDI database.
Catalogue
Search and filter all 3,478 devicesShowing 1-50 of 3,478
Company details
- FDA FEI number
- 3012428435
- Address
- 2300 N Haskell Ave, Dallas, TX, 75204
Frequently asked questions
How many devices does EVOLUTION SPINE, LLC have in the registry?
The registry currently lists 3478 devices for EVOLUTION SPINE, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list EVOLUTION SPINE, LLC's devices?
Among its 50 most recently registered devices, EVOLUTION SPINE, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do EVOLUTION SPINE, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for EVOLUTION SPINE, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from EVOLUTION SPINE, LLC in the registry?
The most recently registered devices listed for EVOLUTION SPINE, LLC include E3D-C Interbody System 130G-XL0706, E3D-C Interbody System 130G-XL0705, E3D-C Interbody System 130G-XL0707 and E3D-C Interbody System 130G-XL0708.