Cimilre Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Cimilre Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CIMILRE Free-T2 Plus
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.
FDA 510(k) Regulatory Record - Cimilre Co., Ltd.
2 devices