# Aspine USA, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: MQV (1)
- Predicates its devices cite: 7 (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
- Wrightmedicaltechnologyinc: 3 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)
- Biocomposites, Ltd.: 1 (https://510kreport.com/company/biocomposites)
- Biomet Orthopedics, Inc.: 1 (https://510kreport.com/company/biomet-orthopedics)

## Firms that cite its devices most
- Gwowei Technology Co., Ltd.: 2 (https://510kreport.com/company/gwowei-technology)
- Ag Digital Technology Corp.: 1 (https://510kreport.com/company/ag-digital-technology)

## Its most-cited devices
- K031319: Osteo-G Bone Void Filler System (2003), cited by 3

## Recent decisions
- K031319: Osteo-G Bone Void Filler System (Jul 17, 2003)

Source page: https://510kreport.com/company/aspine-usa