Coalign Innovations, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
What Coalign Innovations, Inc. makes
Coalign Innovations, Inc. manufactures spinal interbody fusion cages, including the AccuLIF series such as the AccuLIF Cage, AccuLIF TL and PL Cage, AccuLIF TL Cage, AccuLIF TL-PEEK Cage, AccuLIF XL Cage, AccuLIF XL IBF Cage, and AccuLIF TL-PEEK IBF Cage.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Acculif Cage Ref K110270
Regimes: 510(k) Registry: 510(k)Acculif Tl And Pl Cage Ref K132505
Regimes: 510(k) Registry: 510(k)Acculif Tl Cage Ref K121683
Regimes: 510(k) Registry: 510(k)Acculif Tl And Pl Cage Ref K123752
Regimes: 510(k) Registry: 510(k)Acculif Tl-Peek Cage Ref K123281
Regimes: 510(k) Registry: 510(k)Acculif Xl Cage Ref K130194
Regimes: 510(k) Registry: 510(k)Coalign Innovations Acculif Xl Ibf Cage Ref K131443
Regimes: 510(k) Registry: 510(k)Acculif Tl-Peek Ibf Cage Ref K112095
Regimes: 510(k) Registry: 510(k)Acculif Tl Cage Ref K113465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coalign Innovations, Inc. have in the registry?
The registry currently lists 9 devices for Coalign Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coalign Innovations, Inc.'s devices?
Among its 9 most recently registered devices, Coalign Innovations, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Coalign Innovations, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Coalign Innovations, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coalign Innovations, Inc. in the registry?
The most recently registered devices listed for Coalign Innovations, Inc. include ACCULIF CAGE, ACCULIF TL AND PL CAGE, ACCULIF TL CAGE and ACCULIF TL-PEEK CAGE.