Additive Device, Inc. (Adi) D/B/A Restor3D is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Additive Device, Inc. (Adi) D/B/A Restor3D - FDA 510(k) Cleared Devic...
Recent clearances: ADI TiDAL Osteotomy Wedge, ADI Cervical Interbody Fusion Device
2
Total
2
Cleared
0
Denied
Additive Device, Inc. (Adi) D/B/A Restor3D has 2 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Additive Device, Inc. (Adi) D/B/A Restor3D Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Additive Device, Inc. (Adi) D/B/A Restor3D
2 devices