Additive Device, Inc. (Adi) D/B/A Restor3D
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| ADI TiDAL Osteotomy Wedge (K191047) | Additive Device, Inc. (Adi) D/B/A Restor3D | 2019-11-05 |
| ADI Cervical Interbody Fusion Device (K191812) | Additive Device, Inc. (Adi) D/B/A Restor3D | 2019-10-24 |
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