Edson Corp.
Country not established
- Devices
- 1
What Edson Corp. makes
Edson Corp. manufactures the WET SENSE device.
This product is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Wet Sense Ref K935915
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Edson Corp. have in the registry?
The registry currently lists 1 device for Edson Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edson Corp.'s devices?
Among its 1 most recently registered device, Edson Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Edson Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Edson Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Edson Corp. in the registry?
The most recently registered devices listed for Edson Corp. include WET SENSE.