Medical Device Manufacturer · KR , Busan

Neosil Co., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015
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.

FDA 510(k) Regulatory Record - Neosil Co., Ltd.

2 devices
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