Heuron Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Heuron Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Incheon, KR.
Latest FDA clearance: May 2024. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Heuron Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lighten Bridge, LLC and Hogan Lovells US LLP.
5 devices