# Bright Spine

- Location (FDA's records): Boca Raton, FL
- FDA decisions: 3 (2011–2023): 3 510(k) clearances
- Names in FDA's records: Bright Spine (2); Bright Spine, Inc. (1)
- Product codes: PLR (2), ODP (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (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
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Choicespine, LP: 1 (https://510kreport.com/company/choicespine)
- Nexxt Spine, LLC: 1 (https://510kreport.com/company/nexxt-spine)
- Johnson and Johnson: 1 (https://510kreport.com/company/johnson-and-johnson)

## Its most-cited devices
- K192145: Galileo Vertebral Body Replacement Device (2020), cited by 1

## Recent decisions
- K221542: Galileo Vertebral Body Replacement Device (Jan 13, 2023)
- K192145: Galileo Vertebral Body Replacement Device (Apr 21, 2020)
- K102449: Bright Spine Galileo Spinal Spacer System (Feb 11, 2011)

Source page: https://510kreport.com/company/bright-spine