Raymax Medical Corp.
CanadaFDA applicant, unverified
- Devices
- 3
What Raymax Medical Corp. makes
Raymax Medical Corp. manufactures fluoroscopic imaging systems, including the RAYMAX 2100 series (models 2130 and 2136) and the Alpha model, designed for real-time X-ray visualization in medical procedures.
These devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. The company’s products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Raymax 2100 Models 2130 & 2136 Ref K883431
Regimes: 510(k) Registry: 510(k)Video Fluoroscope Ref K914414
Regimes: 510(k) Registry: 510(k)Alpha Ref K930273
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Raymax Medical Corp. have in the registry?
The registry currently lists 3 devices for Raymax Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Raymax Medical Corp.'s devices?
Among its 3 most recently registered devices, Raymax Medical Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Raymax Medical Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Raymax Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Raymax Medical Corp. in the registry?
The most recently registered devices listed for Raymax Medical Corp. include RAYMAX 2100 MODELS 2130 & 2136, VIDEO FLUOROSCOPE and ALPHA.