# Cochlear Bone Anchored Systems AB

- Location (FDA's records): Centennial, CO
- FDA decisions: 2 (2008–2009): 2 510(k) clearances
- Product codes: LXB (1), MAH (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 11 (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
- Entific Medical Systems, Inc.: 2 (https://510kreport.com/company/entific-medical-systems)
- Resound Corp.: 2 (https://510kreport.com/company/resound)
- Cochlear Americas: 1 (https://510kreport.com/company/cochlear-americas)
- Sonix Technologies, Inc.: 1 (https://510kreport.com/company/sonix-technologies)
- Madsen Electronics (Canada), Ltd.: 1 (https://510kreport.com/company/madsen-electronics-canada)

## Firms that cite its devices most
- Cochlear Americas: 4 (https://510kreport.com/company/cochlear-americas)
- Oticon Medical AB: 3 (https://510kreport.com/company/oticon-medical)
- Sonitus Medical, Inc.: 2 (https://510kreport.com/company/sonitus-medical)
- Sophono, Inc.: 1 (https://510kreport.com/company/sophono)

## Its most-cited devices
- K090720: Cochlear Baha BP100 (2009), cited by 7
- K080363: Baha Cordelle II (2008), cited by 4

## Recent decisions
- K090720: Cochlear Baha BP100 (Jun 17, 2009)
- K080363: Baha Cordelle II (Apr 10, 2008)

Source page: https://510kreport.com/company/cochlear-bone-anchored-systems