K1Med Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
K1Med Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Coresculpt & Magsculpt
1
Total
1
Cleared
0
Denied
K1Med Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by K1Med 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 - K1Med Co., Ltd.
1 devices