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