Hemispheres Marketing Co., Ltd.
Country not established
- Devices
- 1
What Hemispheres Marketing Co., Ltd. makes
Hemispheres Marketing Co., Ltd. manufactures the CLASSIQUE, a Class I medical device designed for use in specific clinical applications. The device is intended for low-risk procedures, such as minor surgical instruments or patient monitoring tools.
The CLASSIQUE is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Classique Ref K932899
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemispheres Marketing Co., Ltd. have in the registry?
The registry currently lists 1 device for Hemispheres Marketing Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemispheres Marketing Co., Ltd.'s devices?
Among its 1 most recently registered device, Hemispheres Marketing Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hemispheres Marketing Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemispheres Marketing Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hemispheres Marketing Co., Ltd. in the registry?
The most recently registered devices listed for Hemispheres Marketing Co., Ltd. include CLASSIQUE.