Cimilre Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cimilre Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Last cleared in 2022. Active since 2017. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Cimilre Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
2 devices