Myblend
FranceFDA applicant, unverified
- Devices
- 1
What Myblend makes
Myblend manufactures the myLEDmask, a reusable respiratory protection device designed for filtering airborne particles, including those containing viruses and bacteria.
The myLEDmask 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
myLEDmask Ref K223147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Myblend have in the registry?
The registry currently lists 1 device for Myblend. Devices recorded under merged duplicate company entries are counted once.
Which registries list Myblend's devices?
Among its 1 most recently registered device, Myblend has devices listed in FDA 510(k) (1 device).
What risk classes do Myblend's devices fall under?
Among its 1 most recently registered device, the classes recorded for Myblend's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Myblend in the registry?
The most recently registered devices listed for Myblend include myLEDmask.