Magna Fortis Corporation
Country not established
- Devices
- 1
What Magna Fortis Corporation makes
Magna Fortis Corporation manufactures the Magna Fortis Ophthalmoscope Diagnostic Kit, a device designed for examining the interior structures of the eye during clinical evaluations.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Magna Fortis Ophthalmoscope Diagnostic Kit Ref K002044
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Magna Fortis Corporation have in the registry?
The registry currently lists 1 device for Magna Fortis Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magna Fortis Corporation's devices?
Among its 1 most recently registered device, Magna Fortis Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Magna Fortis Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Magna Fortis Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Magna Fortis Corporation in the registry?
The most recently registered devices listed for Magna Fortis Corporation include MAGNA FORTIS OPHTHALMOSCOPE DIAGNOSTIC KIT.