Dimedi Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Dimedi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Zeroveno
1
Total
1
Cleared
0
Denied
Dimedi Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wonju-Si, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Dimedi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wise Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dimedi Co., Ltd.
1 devices