Medical Device Manufacturer · US , Helsinki Uusimaa , FL

Disior, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2021

Total

Cleared

Denied

Disior, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Helsinki Uusimaa, US.

Latest FDA clearance: Feb 2026. Active since 2021. Primary specialty: Radiology.

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

FDA 510(k) cleared devices by Disior, Ltd.

6 devices

1-6 of 6