Eizo Corporation - FDA 510(k) Cleared Devices
Recent clearances: CuratOR EX2742, RadiForce MX247W, RadiForce GX570
31
Total
31
Cleared
0
Denied
FDA 510(k) Regulatory Record - Eizo Corporation Radiology ✕
28 devices
Cleared
Sep 01, 2026
RadiForce MX247W
Radiology
26d
Cleared
Aug 28, 2025
RadiForce GX570
Radiology
59d
Cleared
Nov 27, 2024
RadiForce RX570
Radiology
51d
Cleared
Jul 16, 2024
RadiForce RX670
Radiology
55d
Cleared
Dec 21, 2023
RadiForce MX317W
Radiology
58d
Cleared
May 12, 2023
RadiForce MX217
Radiology
60d
Cleared
Apr 20, 2023
RadiForce RX270
Radiology
126d
Cleared
May 10, 2022
RadiForce MX243W
Radiology
21d
Cleared
Jul 12, 2021
RadiForce RX370
Radiology
60d
Cleared
Mar 23, 2020
RadiForce RX1270, RadiForce RX1270-AR
Radiology
25d
Cleared
Mar 08, 2019
RadiForce MX216
Radiology
37d
Cleared
Oct 18, 2018
RadiForce RX360, RX360-AR
Radiology
28d