Radisen Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Radisen Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AXIR-CX, PEDRA-1417MC, PEDRA-1417MG, PEDRA-1417FC, PEDRA-1417FG
2
Total
2
Cleared
0
Denied
Radisen Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Anyang-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radisen Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtechgroup as regulatory consultant.
FDA 510(k) Regulatory Record - Radisen Co., Ltd.
2 devices