Medicore Co., Ltd. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Medicore Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: IRIS-XP, MAX PULSE SYSTEM, SA-3000P
3
Total
3
Cleared
0
Denied
Medicore Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Gangnam-Gu, Seoul, KR.
Last cleared in 2021. Active since 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medicore Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Gms Consulting.
FDA 510(k) Regulatory Record - Medicore Co., Ltd.
3 devices