K1Med Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What K1Med Co., Ltd. makes
K1Med Co., Ltd. manufactures non-invasive body contouring devices, including Coresculpt and Magsculpt, which use focused electromagnetic energy to reshape and tone muscle tissue in targeted areas of the body.
These devices are classified as Class II under US regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Coresculpt & Magsculpt Ref K222400
510(k) 510(k)
Frequently asked questions
How many devices does K1Med Co., Ltd. have in the registry?
The registry currently lists 1 device for K1Med Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K1Med Co., Ltd.'s devices?
Among its 1 most recently registered device, K1Med Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do K1Med Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for K1Med Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from K1Med Co., Ltd. in the registry?
The most recently registered devices listed for K1Med Co., Ltd. include Coresculpt & Magsculpt.