Fujifilm Corporaton - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Fujifilm Corporaton has 6 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Last cleared in 2023. Active since 2020.
Browse the FDA 510(k) cleared devices submitted by Fujifilm Corporaton Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Fujifilm Medical Systems U.S.A, Inc. and FUJIFILM Healthcare Americas Corporation.
6 devices
Cleared
Jan 27, 2023
FUJIFILM Endoscope Model EI-740D/S
Gastroenterology & Urology
241d
Cleared
Jan 11, 2023
Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D
Gastroenterology & Urology
77d
Cleared
Nov 10, 2022
FUJIFILM Endoscope Model EB-710P
Ear, Nose, Throat
223d
Cleared
Dec 02, 2021
FUJIFILM Video Laparoscope EL-R740M30
General & Plastic Surgery
77d
Cleared
Jun 30, 2021
Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0
General & Plastic Surgery
191d
Cleared
Aug 27, 2020
Synapse 3D Cardiac Tools
Radiology
136d