Fujifilm Corporation - FDA 510(k) Cleared Devices

Fujifilm Corporation has 63 FDA 510(k) cleared medical devices. Based in Ashigara Kami-Gun, JP.

Latest FDA clearance: May 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 Medical Systems U.S.A, Inc., FUJIFILM Healthcare Americas Corporation and Fujifilm Medical System U.S.A., Inc..