Medi-Flex
Country not established
- Devices
- 1
What Medi-Flex makes
Medi-Flex manufactures the A.W.E.L., a medical device designed for wound care or patient monitoring (specific application not detailed).
The A.W.E.L. is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
A.W.E.L. Ref K943614
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Flex have in the registry?
The registry currently lists 1 device for Medi-Flex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Flex's devices?
Among its 1 most recently registered device, Medi-Flex has devices listed in FDA 510(k) (1 device).
What risk classes do Medi-Flex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medi-Flex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Flex in the registry?
The most recently registered devices listed for Medi-Flex include A.W.E.L..