Eizo Corporation
Eizo Corporation holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026, with 5 FDA device recalls on record.
Top product codes for Eizo Corporation
FDA recalls by Eizo Corporation
- Z-2293-2020 — RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in displaying radiological images (including full-field digital mammography and digital breast tomosynthesis) for review, analysis, and diagnosis by trained medical practitioners.
- Z-2294-2020 — RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.
- Z-2088-2015 — RadiForce RX650, 6MP Color LCD Monitor, Part Code No. 0FTD1957A5, 0FTD195B5, UPC 690592037203. This product is intended to be used in displaying and viewing digital images for review and analysis by trained medical practitioners. It does not support the display of mammography images for diagnosis.
- Z-2089-2015 — RadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180. This product is intended to be used in displaying and viewing digital images those of digital mammography for review and analysis by trained medical practitioners.
- Z-2087-2015 — RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical practitioners.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Eizo Corporation
- K262397 — CuratOR EX2742
- K262783 — RadiForce MX247W
- K252030 — RadiForce GX570; RadiForce GX570-AR
- K242545 — RadiForce MX317W-PA
- K243221 — RadiForce RX570; RadiForce RX570-AR
- K241441 — RadiForce RX670; RadiForce RX670-AR
- K233465 — RadiForce MX317W
- K231066 — CuratOR EX3242-FD
- K230684 — RadiForce MX217
- K223768 — RadiForce RX270
- K221136 — RadiForce MX243W
- K211491 — RadiForce RX370
- K200485 — RadiForce RX1270, RadiForce RX1270-AR
- K190153 — RadiForce MX216
- K182591 — RadiForce RX360, RX360-AR
- K181609 — RadiForce GX560, GX560-AR
- K180961 — RadiForce MX194
- K172738 — RadiForce RX560, RX560-AR
- K170949 — RadiForce MX315W
- K163335 — 6MP Color LCD Monitor, RadiForce RX660, RX660-AR
- K162497 — 5MP Monochrome LCD Monitor, RadiForce GX550, GX550-AR
- K160247 — 2MP Color LCD Monitor, RadiForce RX250 and RX250-AR
- K153354 — 3MP Color LCD Monitor, RadiForce RX350
- K152713 — 8MP Color LCD Monitor, RadiForce RX850, RX850-AR
- K151883 — 5MP Monochrome LCD Monitor, RadiForce GX540
- K150106 — 2MP Color LCD Monitor, RadiForce RS240
- K143261 — 2.3MP Color LCD Monitor, RadiForce MX242W
- K143098 — 3MP Color LCD monitor, RadiForce RS340
- K140702 — 8MP COLOR LCD MONITOR, RADIFORCE RX850
- K134002 — 6MP COLOR LCD MONITOR, RADIFORCE RX650
- K131090 — 2MP COLOR LCD MONITOR, RADIFORCE MX215
Data sourced from openFDA. This site is unofficial and independent of the FDA.