Dk Mungyo Corporation
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What Dk Mungyo Corporation makes
Dk Mungyo Corporation manufactures the Flex Fit, a medical device designed for orthopedic or joint support applications, likely intended to provide adjustable stabilization or mobility assistance.
The Flex Fit 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
Flex Fit Ref K190790
510(k) 510(k)
Frequently asked questions
How many devices does Dk Mungyo Corporation have in the registry?
The registry currently lists 1 device for Dk Mungyo Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dk Mungyo Corporation's devices?
Among its 1 most recently registered device, Dk Mungyo Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Dk Mungyo Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dk Mungyo Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dk Mungyo Corporation in the registry?
The most recently registered devices listed for Dk Mungyo Corporation include Flex Fit.