# Orquest, Inc.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: MQV (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 11 (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
- Interpore Cross Intl.: 2 (https://510kreport.com/company/interpore-cross-intl)
- Orthovita, Inc.: 1 (https://510kreport.com/company/orthovita)
- Interpore Intl.: 1 (https://510kreport.com/company/interpore-intl)
- Geistlich Pharma AG: 1 (https://510kreport.com/company/geistlich-pharma)
- Collagen Matrix, Inc.: 1 (https://510kreport.com/company/collagen-matrix)
- Neucoll, Inc.: 1 (https://510kreport.com/company/neucoll)

## Firms that cite its devices most
- Depuy Spine, Inc.: 4 (https://510kreport.com/company/depuy-spine)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- R and D Medical, LLC: 1 (https://510kreport.com/company/r-and-d-medical)
- Centerpulse Spine-Tech, Inc.: 1 (https://510kreport.com/company/centerpulse-spine-tech)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Collagen Matrix, Inc.: 1 (https://510kreport.com/company/collagen-matrix)
- Beijing Allgens Medical Science & Technology Co, L: 1 (https://510kreport.com/company/beijing-allgens-medical-science-technology-co-l)
- Ossacur AG: 1 (https://510kreport.com/company/ossacur)

## Its most-cited devices
- K012751: Healos Bone Graft Material (2001), cited by 11

## Recent decisions
- K012751: Healos Bone Graft Material (Nov 14, 2001)

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