Fujifilm Corporation - FDA 510(k) Cleared Devices
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
Cleared
Mar 09, 2026
FUJIFILM Endoscope Model ED-S100TP
Gastroenterology & Urology
265d
Cleared
Feb 17, 2026
FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit
Gastroenterology & Urology
357d
Cleared
Feb 06, 2026
Hood DH-084STR
Gastroenterology & Urology
81d
Cleared
Dec 12, 2025
FUJIFILM Ultrasonic Endoscope EB-710US
Ear, Nose, Throat
266d
Cleared
Sep 17, 2025
ECHELON Synergy
Radiology
135d
Cleared
Jun 13, 2025
FUJIFILM Endoscope Model EB-710P
Ear, Nose, Throat
168d
Cleared
Jun 10, 2025
FUJIFILM Endoscope Model EG-840N
Gastroenterology & Urology
210d
Cleared
May 23, 2025
FUJIFILM Endoscope Model EC-860P/M
Gastroenterology & Urology
220d
Cleared
May 21, 2025
Synapse 3D Base Tools (V7.0)
Radiology
166d
Cleared
May 20, 2025
SCENARIA View Phase 5.0
Radiology
99d
Cleared
Apr 11, 2025
FUJIFILM Processor EP-8000
Gastroenterology & Urology
178d
Cleared
Nov 01, 2024
Over-tube (TR-1108A)
Gastroenterology & Urology
32d
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