Winix, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Winix, Inc. makes
Winix, Inc. manufactures the Qorda QD1, a portable air purifier designed to filter airborne particles, allergens, and pollutants from indoor environments using HEPA and activated carbon filtration.
The QD1 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
Qorda QD1 Ref K220990
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Winix, Inc. have in the registry?
The registry currently lists 1 device for Winix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Winix, Inc.'s devices?
Among its 1 most recently registered device, Winix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Winix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Winix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Winix, Inc. in the registry?
The most recently registered devices listed for Winix, Inc. include Qorda QD1.