# Cerabio, LLC

- Location (FDA's records): Prescott, WI
- FDA decisions: 2 (2002–2002): 2 510(k) clearances
- Product codes: MQV (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)
- Interpore Intl.: 1 (https://510kreport.com/company/interpore-intl)

## Firms that cite its devices most
- Biomet, Inc.: 2 (https://510kreport.com/company/biomet)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Its most-cited devices
- K013966: Apatight-TCP Bone Graft Substitute (2002), cited by 2
- K013960: Apatight HA-Bone Graft Substitute (2002), cited by 1

## Recent decisions
- K013960: Apatight HA-Bone Graft Substitute (May 23, 2002)
- K013966: Apatight-TCP Bone Graft Substitute (May 16, 2002)

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