Vieworks Co., Ltd.
Vieworks Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2026.
Top product codes for Vieworks Co., Ltd.
Recent clearances by Vieworks Co., Ltd.
- K260820 — VIVIX-S 4386W (FXRD-4386WA)
- K254092 — Bellalun 2D (VDMS-1000S)
- K251410 — VXvue
- K241113 — VIVIX-M
- K241125 — VIVIX-S 1751S
- K220239 — Solid State X-ray Imager(Model: FXRD-4386WB)
- K221512 — Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW)
- K200418 — VIVIX-S VW
- K190611 — VIVIX-S 1751S
- K181003 — VIVIX-S 1717V
- K163703 — VIVIX-S 1417N
- K161113 — QXLink
- K152855 — VIVIX-S 1012N
- K152894 — VIVIX-S 1717N
- K132302 — QXLINK
- K122865 — VIVIX-S WIRELESS
- K122866 — VIVIX-S WITH VXVUE
- K120020 — VIVIX-S
- K092081 — QXLINK
- K080553 — DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16
- K073056 — DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9
Data sourced from openFDA. This site is unofficial and independent of the FDA.