Corisen Group, Ltd.
Country not established
- Devices
- 1
What Corisen Group, Ltd. makes
Corisen Group, Ltd. manufactures the Worry-Remover Irrigator, a Class I medical device designed for irrigation purposes in clinical settings.
The Worry-Remover Irrigator is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Worry-Remover Irrigator Ref K030056
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corisen Group, Ltd. have in the registry?
The registry currently lists 1 device for Corisen Group, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corisen Group, Ltd.'s devices?
Among its 1 most recently registered device, Corisen Group, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Corisen Group, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Corisen Group, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Corisen Group, Ltd. in the registry?
The most recently registered devices listed for Corisen Group, Ltd. include WORRY-REMOVER IRRIGATOR.