Seilglobal Co., Ltd. is one of 459 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Seilglobal Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DentiAnn Smart Sil
1
Total
1
Cleared
0
Denied
Seilglobal Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Busan, KR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Seilglobal Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Seilglobal Co., Ltd.
1 devices