Hayday Irrit-Easer
Country not established
- Devices
- 1
What Hayday Irrit-Easer makes
Hayday Irrit-Easer produces a handheld device called the Irrit-Easer Wand, designed for topical skin applications to reduce irritation or discomfort.
The Irrit-Easer Wand is classified as a Class I medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hayday Irrit-Easer Wand Ref K840035
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hayday Irrit-Easer have in the registry?
The registry currently lists 1 device for Hayday Irrit-Easer. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hayday Irrit-Easer's devices?
Among its 1 most recently registered device, Hayday Irrit-Easer has devices listed in FDA 510(k) (1 device).
What risk classes do Hayday Irrit-Easer's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hayday Irrit-Easer's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hayday Irrit-Easer in the registry?
The most recently registered devices listed for Hayday Irrit-Easer include HAYDAY IRRIT-EASER WAND.