Medical Device Manufacturer · JP , Ashigara Kami-Gun

Fujifilm Corporation - FDA 510(k) Cleared Devices

60 submissions · 60 cleared · Since 2018
60
Total
60
Cleared
0
Denied

Fujifilm Corporation has 60 FDA 510(k) cleared medical devices. Based in Ashigara Kami-Gun, JP.

Latest FDA clearance: Mar 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.

FDA 510(k) cleared devices by Fujifilm Corporation

60 devices
1-12 of 60

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