Cogent Spine, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Cogent Spine, LLC makes
Cogent Spine, LLC manufactures spinal interbody fusion devices, including the COGENT MED-LIF XL and MED-LIF systems for anterior lumbar interbody fusion, as well as the Cogent Lateral Interbody System for lateral approaches. These products are designed for use in surgical procedures to stabilize the spine and promote fusion in the lumbar region.
The company’s portfolio is classified under FDA Class II devices and is authorised through the 510(k) clearance pathway. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cogent Med-Lif Xl Ref K142193
Regimes: 510(k) Registry: 510(k)Cogent Med-Lif Ref K132738
Regimes: 510(k) Registry: 510(k)Cogent Lateral Interbody System Ref K151406
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cogent Spine, LLC have in the registry?
The registry currently lists 3 devices for Cogent Spine, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cogent Spine, LLC's devices?
Among its 3 most recently registered devices, Cogent Spine, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Cogent Spine, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cogent Spine, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cogent Spine, LLC in the registry?
The most recently registered devices listed for Cogent Spine, LLC include COGENT MED-LIF XL, COGENT MED-LIF and Cogent Lateral Interbody System.