Medical Device Manufacturer · CN , Shen Zhen

Shenzhen Viatom Technology Co., Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2019

Total

Cleared

Denied

Shenzhen Viatom Technology Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Shen Zhen, CN.

Latest FDA clearance: Feb 2025. Active since 2019. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Shenzhen Viatom Technology Co., Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Shenzhen Joyantech Consulting Co., Ltd., Mdi Consultants, Inc. and Irc.

Shenzhen Viatom Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Shenzhen Viatom Technology Co., Ltd.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 04, 2026