Winix, Inc. - FDA 510(k) Cleared Devices

Winix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hwaseong-Si, KR.

Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Winix, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Withus Group, Inc. as regulatory consultant.