Medical Device Manufacturer · KR , Ulsan Gwangyeogsi

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

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

Unilam Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Ulsan Gwangyeogsi, KR.

Last cleared in 2023. Active since 2015. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Unilam Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Allura Medical Solutions, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Unilam Co., Ltd.
2 devices
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