# Additive Device, Inc. (Adi) D/B/A Restor3D

- Location (FDA's records): Durham, NC
- FDA decisions: 2 (2019–2019): 2 510(k) clearances
- Product codes: ODP (1), PLF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)
- Ascension Orthopedic: 1 (https://510kreport.com/company/ascension-orthopedic)

## Firms that cite its devices most
- Spinepoint, LLC: 1 (https://510kreport.com/company/spinepoint)
- Restor3D: 1 (https://510kreport.com/company/restor3d)
- Global Biomedica s.r.o.: 1 (https://510kreport.com/company/global-biomedica)

## Its most-cited devices
- K191812: ADI Cervical Interbody Fusion Device (2019), cited by 2
- K191047: ADI TiDAL Osteotomy Wedge (2019), cited by 1

## Recent decisions
- K191047: ADI TiDAL Osteotomy Wedge (Nov 5, 2019)
- K191812: ADI Cervical Interbody Fusion Device (Oct 24, 2019)

Source page: https://510kreport.com/company/additive-device-adi-d-b-a-restor3d