BLUECORE COMPANY Co., Ltd. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
BLUECORE COMPANY Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PicoreMax (PicoreMax), Lasya-Trinity, ZenPro 40
3
Total
3
Cleared
0
Denied
BLUECORE COMPANY Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Busan, KR.
Latest FDA clearance: Sep 2026. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by BLUECORE COMPANY Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bio-Med USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - BLUECORE COMPANY Co., Ltd.
3 devices