Medical Device Manufacturer · US , Buena Park , CA

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

14 submissions · 14 cleared · Since 2011
14
Total
14
Cleared
0
Denied

Daesung Maref Co., Ltd. has 14 FDA 510(k) cleared medical devices. Based in Buena Park, US.

Last cleared in 2023. Active since 2011. Primary specialty: Physical Medicine.

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

510(k) submissions have been managed by Global Medical Standard Consulting Co., Ltd. as regulatory consultant.

FDA 510(k) Regulatory Record - Daesung Maref Co., Ltd.
14 devices
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