Crown Aesthetics | Premier Aesthetic Innovations for Leading Practices

Crown AestheticsBellus Medical2024-03-04T21:55:10-05:00

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CROWN AESTHETICS BREAKTHROUGH TECHNOLOGY BIOJUVE™ NOW AVAILABLE

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INTRODUCING:
SkinPen® Precision Premium Biocellulose Masque

Crown Aesthetics Creates “Gateway” Microneedling, Platelet-Rich Plasma PRP and Skin Biome Care Technology That Draws New Patients to Leading Physician-Directed Practices Around the World.

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Crown Aesthetics Creates “Gateway” Microneedling, Platelet-Rich Plasma, and Light-Activated Cream Innovations That Draw New Patients to Leading Physician-Directed Practices Around the World.

Become A Provider

Beauty expert Cheryl Kramer Kaye reviews SkinPen and shares why she loves the First FDA-cleared microneedling device.

CROWN’S INNOVATIVE LINEUP

Crown Aesthetics products deliver rejuvenation and restoration to your patients. And your bottom line.

SKINPEN^®

The First FDA-Cleared Microneedling
Device in the World¹

BIOJUVE^TM

Breakthrough skin science that optimizes skin health on and below the surface.

PROGEN PRP^TM

Flexible Platelet-Rich Plasma System²

MEDIA COVERAGE + INDUSTRY RECOGNITION

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References
[1] SkinPen® U.S. intended use: The SkinPen® Precision system is a microneedling device and accessories intended to be used as a treatment to improve the appearance of wrinkles of the neck for Fitzpatrick skin types II – IV and to improve the appearance of facial acne scars in adults with all Fitzpatrick skin types aged 22 years and older. Rx only. SkinPen® international intended use: SkinPen Precision is a microneedling device that utilizes collagen induction therapy to treat melasma, acne, and surgical scars. See intended use, important safety information, and clinical trial details (data on file) at skinpen.com. [2] ProGen™ intended use: The ProGen PC Kit is indicated for the rapid preparation of autologous Platelet Rich Plasma from a small sample of blood at the patient’s point of care. The Platelet Rich Plasma is mixed with autograft/or allograft bone prior to the application to a bony defect for improving handling characteristics of the graft. Results based on a survey conducted by patients after three procedures spaced four weeks apart.