Saeyang Microtech Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Saeyang Microtech Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Last cleared in 2022. Active since 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Saeyang Microtech Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
4 devices