# Vivaray, Inc.

- Location (FDA's records): Portola Valley, CA
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: JAQ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Biolucent, Inc.: 1 (https://510kreport.com/company/biolucent)
- Nucletron-Oldelft Corp.: 1 (https://510kreport.com/company/nucletron-oldelft)

## Firms that cite its devices most
- Gc Medtech, LLC: 1 (https://510kreport.com/company/gc-medtech)
- Radiadyne, LLC (Specification Developer): 1 (https://510kreport.com/company/radiadyne-specification-developer)

## Its most-cited devices
- K092822: Capri Applicator (2009), cited by 2

## Recent decisions
- K092822: Capri Applicator (Nov 3, 2009)

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