Medmix Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medmix Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Smartlux Mini
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