Fujifilm Corporation - FDA 510(k) Cleared Devices

Fujifilm Corporation has 62 FDA 510(k) cleared medical devices. Based in Ashigara Kami-Gun, JP.

Latest FDA clearance: Apr 2026. Active since 2018. Primary specialty: Gastroenterology & Urology.

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

Regulatory submissions have been managed by FUJIFILM Healthcare Americas Corporation, Fujifilm Medical Systems U.S.A, Inc. and Fujiflm Medical Systems U.S.A., Inc..