# Spinepoint, LLC

- Location (FDA's records): Reno, NV
- FDA decisions: 1 (2026–2026): 1 510(k) clearance
- Product codes: ODP (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Additive Device, Inc. (Adi) D/B/A Restor3D: 1 (https://510kreport.com/company/additive-device-adi-d-b-a-restor3d)

## Recent decisions
- K252432: Flex-Z™ Cervical Cage (Mar 25, 2026)

Source page: https://510kreport.com/company/spinepoint