Medical Device Manufacturer · US , Sunrise , FL

Venus Concept USA, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2014

Recent clearances: AI.ME System, Venus BlissMAX, Venus BlissMAX

11
Total
11
Cleared
0
Denied

Venus Concept USA, Inc. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Sunrise, US.

Last cleared in 2022. Active since 2014.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by BioVision , Ltd. as regulatory consultant.

FDA 510(k) Regulatory Record - Venus Concept USA, Inc.

11 devices
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