Yomura Technologies, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Yomura Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Clicky Cross
2
Total
2
Cleared
0
Denied
Yomura Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Taipei City, TW.
Last cleared in 2022. Active since 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Yomura Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Zhengcheng Consulting Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Yomura Technologies, Inc.
2 devices