Neosil Co., Ltd. is one of 448 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Neosil Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PEAK NS033CF, PEAK NS017CF, PEAK
2
Total
2
Cleared
0
Denied
Neosil Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Busan, KR.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Neosil Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by LK Consulting Group USA, Inc. and Onbix Corporation.
FDA 510(k) Regulatory Record - Neosil Co., Ltd.
2 devices