Magnettx Oncology Solutions, Ltd.
CanadaFDA applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Magnettx Oncology Solutions, Ltd. makes
Magnettx Oncology Solutions, Ltd. manufactures the Aurora-RT, a radiation therapy planning and treatment system designed to enhance precision in external beam radiotherapy for cancer treatment.
The company’s portfolio is regulated under FDA’s Class II device category and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Aurora-RT Ref K213526
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Magnettx Oncology Solutions Ltd Edmonton Alberta · CA FEI 3016591365
Frequently asked questions
How many devices does Magnettx Oncology Solutions, Ltd. have in the registry?
The registry currently lists 1 device for Magnettx Oncology Solutions, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magnettx Oncology Solutions, Ltd.'s devices?
Among its 1 most recently registered device, Magnettx Oncology Solutions, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Magnettx Oncology Solutions, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Magnettx Oncology Solutions, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Magnettx Oncology Solutions, Ltd. in the registry?
The most recently registered devices listed for Magnettx Oncology Solutions, Ltd. include Aurora-RT.
Which FDA establishments are linked to Magnettx Oncology Solutions, Ltd.?
1 FDA establishment is linked to Magnettx Oncology Solutions, Ltd. in the registry; they are listed on the company page.