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

Skia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.

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

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

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.