Venus Concept Receives FDA 510(k) Clearance of Venus BlissMAX
Venus Concept Inc announces it has received 510(k) clearance from the US Food and Drug Administration to market the Venus BlissMAX device in the United States.
Venus Concept Inc announces it has received 510(k) clearance from the US Food and Drug Administration to market the Venus BlissMAX device in the United States.
The American Society of Plastic Surgeons (ASPS) has released supplemental data for its 2022 procedural statistics, revealing generational trends, increasing male interest in minimally invasive procedures, and fluctuating surgeon fees, with an emphasis on safety and authenticity in the pursuit of beauty and self-confidence.