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

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.

510(k) submissions have been managed by Paragon 28, Inc. as regulatory consultant.