Terumo Corporation - FDA 510(k) Cleared Devices

Terumo Corporation has 13 FDA 510(k) cleared medical devices. Based in Shibuya-Ku, Tokyo, JP.

Latest FDA clearance: Mar 2026. Active since 2012. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Terumo Medical Corporation as regulatory consultant.