Cimilre Co., Ltd. is one of 440 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 Dual Max, CIMILRE Free-T2 Plus, CIMLRE F1 and CIMILRE S3
3
Total
3
Cleared
0
Denied
Cimilre Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Latest FDA clearance: Aug 2026. 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.
Regulatory submissions have been managed by Third Party Review Group, LLC and GMSC Co., Ltd..
FDA 510(k) Regulatory Record - Cimilre Co., Ltd.
3 devices