Medical Device Manufacturer · US , Pittsburgh , PA

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

2 submissions · 2 cleared · Since 2012
2
Total
2
Cleared
0
Denied

Medmix Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.

Last cleared in 2022. Active since 2012. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Gms Consulting as regulatory consultant.

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