# Viewray, Incorporated

- Location (FDA's records): Oakwood Village, OH
- FDA decisions: 6 (2011–2021): 6 510(k) clearances
- Product codes: IYE (5), MUJ (1)
- 510(k) review time since 2016: median 136 days, against 90 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 9 (6 its own); citations of its devices by later devices: 9 (6 its own)
- Recalls linked to its devices: 12 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Varian Medical Systems, Inc.: 3 (https://510kreport.com/company/varian-medical-systems)

## Firms that cite its devices most
- Elekta, Ltd.: 2 (https://510kreport.com/company/elekta)
- Magnettx Oncology Solutions, Ltd.: 1 (https://510kreport.com/company/magnettx-oncology-solutions)

## Its most-cited devices
- K170751: MRIdian Linac System with 138-leaf Collimator (2017), cited by 3
- K162393: The ViewRay (MRIdian) Linac System (2017), cited by 2
- K102915: Viewray Treatment Planning and Delivery System (2011), cited by 2
- K111862: Viewray System (2012), cited by 1
- K181989: MRIdian Linac System (2019), cited by 1

## Recent decisions
- K212958: MRIdian Linac System (Dec 14, 2021)
- K181989: MRIdian Linac System (Feb 20, 2019)
- K170751: MRIdian Linac System with 138-leaf Collimator (Jun 7, 2017)
- K162393: The ViewRay (MRIdian) Linac System (Feb 24, 2017)
- K111862: Viewray System (May 22, 2012)
- K102915: Viewray Treatment Planning and Delivery System (Jan 12, 2011)

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