Eizo Corporation

FDA Regulatory Profile

Eizo Corporation appears in FDA public data with 5 recalls, 31 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2293-2020, Class II) was initiated on Jul 30, 2019. Its most recent 510(k) clearance was granted on Sep 11, 2026.

Summary

Total Recalls
5
510(k) Clearances
31
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2293-2020Class IIRadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated fJul 30, 2019
Z-2294-2020Class IIRadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displayJul 30, 2019
Z-2088-2015Class IIRadiForce RX650, 6MP Color LCD Monitor, Part Code No. 0FTD1957A5, 0FTD195B5, UPC 690592037203. ThisJul 7, 2015
Z-2089-2015Class IIRadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180. This product isJul 7, 2015
Z-2087-2015Class IIRadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 6Jul 7, 2015

Recent 510(k) Clearances

K-NumberDeviceDate
K262397CuratOR EX2742Sep 11, 2026
K262783RadiForce MX247WSep 1, 2026
K252030RadiForce GX570; RadiForce GX570-ARAug 28, 2025
K242545RadiForce MX317W-PAMay 23, 2025
K243221RadiForce RX570; RadiForce RX570-ARNov 27, 2024
K241441RadiForce RX670; RadiForce RX670-ARJul 16, 2024
K233465RadiForce MX317WDec 21, 2023
K231066CuratOR EX3242-FDDec 18, 2023
K230684RadiForce MX217May 12, 2023
K223768RadiForce RX270Apr 20, 2023
K221136RadiForce MX243WMay 10, 2022
K211491RadiForce RX370Jul 12, 2021
K200485RadiForce RX1270, RadiForce RX1270-ARMar 23, 2020
K190153RadiForce MX216Mar 8, 2019
K182591RadiForce RX360, RX360-AROct 18, 2018
K181609RadiForce GX560, GX560-ARAug 24, 2018
K180961RadiForce MX194May 10, 2018
K172738RadiForce RX560, RX560-ARNov 8, 2017
K170949RadiForce MX315WApr 27, 2017
K1633356MP Color LCD Monitor, RadiForce RX660, RX660-ARDec 15, 2016