Medical Device Manufacturer · SE , Malmo

Duearity AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

1

Total

1

Cleared

0

Denied

Duearity AB has 1 FDA 510(k) cleared medical devices. Based in Malmo, SE.

Last cleared in 2023. Active since 2023. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Duearity AB Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Duearity AB

1 devices

1-1 of 1

Cleared Jun 30, 2023

Tinearity G1 (6103)

Ear, Nose, Throat · 203d