# Angstrom Medica, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: MQV (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Novabone Products, LLC: 1 (https://510kreport.com/company/novabone-products)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Orthovita, Inc.: 1 (https://510kreport.com/company/orthovita)
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)

## Firms that cite its devices most
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)

## Its most-cited devices
- K050025: Nanoss Bone Void Filler (2005), cited by 1

## Recent decisions
- K050025: Nanoss Bone Void Filler (Feb 3, 2005)

Source page: https://510kreport.com/company/angstrom-medica