Viewray, Incorporated
Viewray, Incorporated holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2021, with 6 FDA device recalls on record.
Top product codes for Viewray, Incorporated
FDA recalls by Viewray, Incorporated
- Z-1309-2016 — MRIdian ViewRay Radiation Therapy System, ViewRay Treatment Planning and Delivery System (also known as the MRIdian¿ System) is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated
- Z-0806-2016 — MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc.
- Z-0115-2016 — MRIdian¿ ViewRay¿ Radiation Therapy System, ViewRay¿ Is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
- Z-1954-2015 — Treatment Planning and Delivery System Software version 3.6. ViewRay. Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
- Z-2085-2015 — Patient Handling System (Motion Control Software), Product Usage: Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
- Z-1580-2015 — ViewRay System, Radiation Therapy System
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Viewray, Incorporated
Data sourced from openFDA. This site is unofficial and independent of the FDA.