Venus Concept Snags 510(k) Clearance for Skin Rejuvenation Device

The FDA has granted 510(k) clearance to Venus Concept’s new skin rejuvenation device for ablation and resurfacing of the skin. 

The Venus Viva MD is a portable tabletop device for use in noninvasive skin rejuvenation treatments for patients with a wide range of skin types. The system also collects technical information to help providers improve the efficiency of their treatments.

The company plans a limited launch of the product by the end of the third quarter.