# Binder Biomedical, Inc.

- Location (FDA's records): Boca Raton, FL
- FDA decisions: 2 (2010–2013): 2 510(k) clearances
- Product codes: MAX (1), OVD (1)
- Predicates its devices cite: 5 (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
- Biomet Spine: 1 (https://510kreport.com/company/biomet-spine)
- Biomet Spine & Bone Healing Technologies: 1 (https://510kreport.com/company/biomet-spine-bone-healing-technologies)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Surgicraft, Ltd.: 1 (https://510kreport.com/company/surgicraft)

## Firms that cite its devices most
- Vallum Corporation: 1 (https://510kreport.com/company/vallum)

## Its most-cited devices
- K093015: Binder Intervertebral Body Fusion Device (2010), cited by 2

## Recent decisions
- K130641: Logic Stand-Alone Intervertebral Body Fusion Device (Sep 13, 2013)
- K093015: Binder Intervertebral Body Fusion Device (Feb 25, 2010)

Source page: https://510kreport.com/company/binder-biomedical