# Allosource, Inc.

- Location (FDA's records): Centennial, CO
- FDA decisions: 4 (2008–2023): 4 510(k) clearances
- Names in FDA's records: Allosource, Inc. (2); Allosource (2)
- Product codes: MQV (2), GAT (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 3 (1 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
- Isotis Orthobiologics, Inc.: 3 (https://510kreport.com/company/isotis-orthobiologics)
- Arthrex, Inc.: 2 (https://510kreport.com/company/arthrex)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Firms that cite its devices most
- Rti Surgical, Inc.: 1 (https://510kreport.com/company/rti-surgical)
- Musculoskeletal Transplant Foundation: 1 (https://510kreport.com/company/musculoskeletal-transplant-foundation)

## Its most-cited devices
- K170957: ReConnex Pre-Sutured Tendon (2018), cited by 2
- K071849: Allofuse Gel and Putty (2008), cited by 1

## Recent decisions
- K213046: AceConnex Pre-Sutured Fascia (Jun 27, 2023)
- K170957: ReConnex Pre-Sutured Tendon (Mar 20, 2018)
- K103036: Allofuse Plus (Jan 10, 2011)
- K071849: Allofuse Gel and Putty (Dec 4, 2008)

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