Medical Device Manufacturer · KR , Seoul

Ulike Co., Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
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
1-3 of 3
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