Vieworks Co., Ltd. - FDA 510(k) Cleared Devices

Vieworks Co., Ltd. has 19 FDA 510(k) cleared radiology devices. Based in Gyeonggi-Do, KR.

Latest FDA clearance: Nov 2025. Active since 2007.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.