# Biostructures, LLC

- Location (FDA's records): Newport Beach, CA
- FDA decisions: 5 (2010–2016): 5 510(k) clearances
- Names in FDA's records: Biostructures, LLC (4); Biostructures (1)
- Product codes: MQV (5)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 8 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Novabone Products, LLC: 2 (https://510kreport.com/company/novabone-products)
- Biomatlante: 2 (https://510kreport.com/company/biomatlante)
- Orthovita, Inc.: 2 (https://510kreport.com/company/orthovita)
- Apatech, Ltd.: 1 (https://510kreport.com/company/apatech)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Firms that cite its devices most
- Bioventus, LLC: 3 (https://510kreport.com/company/bioventus)
- Kuros Biosciences B.V: 1 (https://510kreport.com/company/kuros-biosciences-b-v)
- Ventris Medical: 1 (https://510kreport.com/company/ventris-medical)

## Its most-cited devices
- K112857: Interface Bone Void Filler (2011), cited by 2
- K132071: Bioactive Bone Graft Putty (2014), cited by 2
- K142276: MCS Bone Graft (2015), cited by 2
- K092541: Interface (2010), cited by 1
- K160446: MCP Bone Putty (2016), cited by 1

## Recent decisions
- K160446: MCP Bone Putty (Nov 7, 2016)
- K142276: MCS Bone Graft (Jan 16, 2015)
- K132071: Bioactive Bone Graft Putty (Jan 10, 2014)
- K112857: Interface Bone Void Filler (Dec 13, 2011)
- K092541: Interface (Nov 9, 2010)

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