Curiteva, LLC
United StatesFDA applicant, unverified FDA FEI 3012131184
Curiteva, LLC is a medical device manufacturer, with 1,936 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 1,936
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 1,922
- FDA 510(k) 15
- Device classes
- FDA Class II 1,936
- Identifiers
- FDA FEI 3012131184
At a glance
Market reach
- United States
- FDA FEI
What Curiteva, LLC makes
Curiteva, LLC manufactures spinal fusion devices including polymeric and metallic interbody fusion cages, spinal fixation plates, bone-screw internal spinal fixation systems, sacroiliac joint fusion implants, and surgical implant holders. Their product portfolio also includes orthopaedic implant inserters/extractors, bone taps, and navigation systems for spinal procedures.
The company's devices are classified as Class II and listed in the FDA Unique Device Identification (UDI) registry.
Catalogue
Search and filter all 1,936 devicesShowing 1-50 of 1,936
Company details
- FDA FEI number
- 3012131184
- Address
- 25127 WILL MCCOMB DR, Tanner, AL, 35671
Frequently asked questions
How many devices does Curiteva, LLC have in the registry?
The registry currently lists 1936 devices for Curiteva, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curiteva, LLC's devices?
Among its 50 most recently registered devices, Curiteva, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do Curiteva, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Curiteva, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curiteva, LLC in the registry?
The most recently registered devices listed for Curiteva, LLC include Savant Lumbar Interbody Fusion System C295-1000, Acumen Thoracolumbar Plate System C1155-156, Prodigy Pedicle Screw System C525-1300 and Inspire Lumbar Interbody Fusion System C284-302412-12.