Medical Device Manufacturer · KR , Daegu

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

11 submissions · 11 cleared · Since 2018
11
Total
11
Cleared
0
Denied

Finemedix Co., Ltd. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Daegu, KR.

Latest FDA clearance: Apr 2026. Active since 2018.

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

Regulatory submissions have been managed by LK Consulting Group USA, Inc., Withus Group, Inc. and KMC, Inc..

FDA 510(k) Regulatory Record - Finemedix Co., Ltd.
11 devices
1-11 of 11
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