Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Vieworks Co., Ltd.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories3
Latest Approval2025-11-04
TypeNumberDevice NameCodeDate
510(k) K251410 VXvue LLZ 2025-11-04 View
510(k) K241113 VIVIX-M MUE 2025-01-16 View
510(k) K241125 VIVIX-S 1751S MQB 2024-11-15 View
510(k) K220239 Solid State X-ray Imager(Model: FXRD-4386WB) MQB 2022-09-13 View
510(k) K221512 Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW) MQB 2022-07-20 View
510(k) K200418 VIVIX-S VW MQB 2020-03-18 View
510(k) K190611 VIVIX-S 1751S MQB 2019-04-08 View
510(k) K181003 VIVIX-S 1717V MQB 2018-05-15 View
510(k) K163703 VIVIX-S 1417N MQB 2017-02-08 View
510(k) K161113 QXLink LLZ 2016-08-05 View
510(k) K152894 VIVIX-S 1717N MQB 2016-02-26 View
510(k) K152855 VIVIX-S 1012N MQB 2016-02-26 View