Additive Device, Inc. (Adi) D/B/A Restor3D
United StatesFDA applicant, unverified
- Devices
- 2
What Additive Device, Inc. (Adi) D/B/A Restor3D makes
Restor3D specializes in spinal implant devices, including the ADI Cervical Interbody Fusion Device for cervical spine stabilization and the ADI TiDAL Osteotomy Wedge for bone reshaping in orthopedic procedures.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
ADI Cervical Interbody Fusion Device Ref K191812
Regimes: 510(k) Registry: 510(k)ADI TiDAL Osteotomy Wedge Ref K191047
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Additive Device, Inc. (Adi) D/B/A Restor3D have in the registry?
The registry currently lists 2 devices for Additive Device, Inc. (Adi) D/B/A Restor3D. Devices recorded under merged duplicate company entries are counted once.
Which registries list Additive Device, Inc. (Adi) D/B/A Restor3D's devices?
Among its 2 most recently registered devices, Additive Device, Inc. (Adi) D/B/A Restor3D has devices listed in FDA 510(k) (2 devices).
What risk classes do Additive Device, Inc. (Adi) D/B/A Restor3D's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Additive Device, Inc. (Adi) D/B/A Restor3D's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Additive Device, Inc. (Adi) D/B/A Restor3D in the registry?
The most recently registered devices listed for Additive Device, Inc. (Adi) D/B/A Restor3D include ADI Cervical Interbody Fusion Device and ADI TiDAL Osteotomy Wedge.