# Spinal Edge, LLC

- Location (FDA's records): Avon, OH
- FDA decisions: 3 (2006–2010): 3 510(k) clearances
- Product codes: MNH (1), MQP (1), MAX (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 2 (1 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
- Depuyacromed: 4 (https://510kreport.com/company/depuyacromed)
- Depuy Motech Acromed: 2 (https://510kreport.com/company/depuy-motech-acromed)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Lanx, Inc.: 1 (https://510kreport.com/company/lanx)

## Firms that cite its devices most
- Everest Spine, LLC: 1 (https://510kreport.com/company/everest-spine)

## Its most-cited devices
- K091110: Spinal Edge Titan Pedicle Screw System (2009), cited by 1
- K060916: Atlas Spinal Cage, Models SC-150-007, 009, 011, 013, 015, 017. (2006), cited by 1

## Recent decisions
- K092774: Atlas Intervertebral Body Cage (Feb 2, 2010)
- K091110: Spinal Edge Titan Pedicle Screw System (Jul 24, 2009)
- K060916: Atlas Spinal Cage, Models SC-150-007, 009, 011, 013, 015, 017. (Jun 8, 2006)

Source page: https://510kreport.com/company/spinal-edge