Medical Device Manufacturer · JP , Tokyo

Fujifilm Corporaton - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2020

Total

Cleared

Denied

FDA 510(k) Regulatory Record - Fujifilm Corporaton Ear, Nose, Throat ✕

1 devices

1-1 of 1

Regulatory consultants 510(k) submission support ecosystem

Fujifilm Medical Systems U.S.A, Inc.

FUJIFILM Healthcare Americas Corporation

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 15, 2026