# Corespine Technologies, LLC

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: HRX (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
- Endius, Inc.: 1 (https://510kreport.com/company/endius)
- Clarus Medical, LLC: 1 (https://510kreport.com/company/clarus-medical)
- Hydrocision, Inc.: 1 (https://510kreport.com/company/hydrocision)

## Recent decisions
- K090303: Xtend-ST Nucleus Removal System, Model 9004 (Apr 30, 2009)

Source page: https://510kreport.com/company/corespine-technologies