# Kasios Biomaterials

- Location (FDA's records): Temecula, CA
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: MQV (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic: 1 (https://510kreport.com/company/linacol-muh-dan-kim-cev-tek-med-ith-ihr-san-ve-tic)
- Atpac Medical, LLC: 1 (https://510kreport.com/company/atpac-medical)
- Spinecraft, LLC: 1 (https://510kreport.com/company/spinecraft)

## Its most-cited devices
- K042340: Kasios TCP (2004), cited by 3

## Recent decisions
- K042340: Kasios TCP (Nov 24, 2004)

Source page: https://510kreport.com/company/kasios-biomaterials