K-Mot, Inc.
Country not established
- Devices
- 1
What K-Mot, Inc. makes
K-Mot, Inc. manufactures the HARIKY (Model GK-7), a device designed for knee rehabilitation and mobility assistance, aiding patients in controlled range-of-motion exercises.
The HARIKY (Model GK-7) is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hariky, Model Gk-7 Ref K860772
510(k) 510(k)
Frequently asked questions
How many devices does K-Mot, Inc. have in the registry?
The registry currently lists 1 device for K-Mot, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K-Mot, Inc.'s devices?
Among its 1 most recently registered device, K-Mot, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do K-Mot, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for K-Mot, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from K-Mot, Inc. in the registry?
The most recently registered devices listed for K-Mot, Inc. include HARIKY, MODEL GK-7.