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Vieworks Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251410VXvueNovember 4, 2025
K241113VIVIX-MJanuary 16, 2025
K241125VIVIX-S 1751SNovember 15, 2024
K220239Solid State X-ray Imager(Model: FXRD-4386WB)September 13, 2022
K221512Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW)July 20, 2022
K200418VIVIX-S VWMarch 18, 2020
K190611VIVIX-S 1751SApril 8, 2019
K181003VIVIX-S 1717VMay 15, 2018
K163703VIVIX-S 1417NFebruary 8, 2017
K161113QXLinkAugust 5, 2016
K152855VIVIX-S 1012NFebruary 26, 2016
K152894VIVIX-S 1717NFebruary 26, 2016
K132302QXLINKSeptember 12, 2013
K122865VIVIX-S WIRELESSFebruary 1, 2013
K122866VIVIX-S WITH VXVUEJanuary 11, 2013
K120020VIVIX-SMay 4, 2012
K092081QXLINKJuly 21, 2009
K080553DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16April 16, 2008
K073056DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9November 13, 2007