Additive Device, Inc. (Adi) D/B/A Restor3D
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K191047 | ADI TiDAL Osteotomy Wedge | November 5, 2019 |
| K191812 | ADI Cervical Interbody Fusion Device | October 24, 2019 |