Medical Device Manufacturer · US , Eden Prairie , MN

Alliqua Biomedical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016
2
Total
2
Cleared
0
Denied

Alliqua Biomedical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.

Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Alliqua Biomedical, Inc. Filter by specialty or product code using the sidebar.

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All2 General & Plastic Surgery 2