Taeyeon Medical Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Taeyeon Medical Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Dyflex-II, Balex bone Expander System
3
Total
3
Cleared
0
Denied
Taeyeon Medical Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Incheon, KR.
Last cleared in 2022. Active since 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Taeyeon Medical 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 - Taeyeon Medical Co., Ltd.
3 devices