Keosan Trading Co. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Keosan Trading Co. - FDA 510(k) Cleared Devices
Recent clearances: MISTI Silicone Implant, FITme Customized Silicone Implant
2
Total
2
Cleared
0
Denied
Keosan Trading Co. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Jul 2024. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Keosan Trading Co. 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 - Keosan Trading Co.
2 devices