Ulike Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ulike Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W), Diamond Air+ (UI04A, UI04B, UI04C), IPL Hair Removal Device
3
Total
3
Cleared
0
Denied
Ulike Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Oct 2024. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ulike Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Purevisionai, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ulike Co., Ltd.
3 devices