Find Out How EstheCeuticals®
Benefit Your Practice & Your Clients
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Biolock™ cartridge stops leaks.
Four nosecones can be autoclave sterilized.
Two powerful, efficient motor units
Both cordless and corded options
• TWO Microneedling Devices
• FOUR autoclave sterilizable nosecones
• TWO Rechargeable Lithium Batteries
•TWO Power Options: BOTH Corded and Cordless
• TWO year Warranty
• 40 Biolock™ Needle Cartridges
• 40 Client Brochures
• 4 FULL size (30 ml) EstheCeutical® treatment products developed SPECIFICALLY for microneedling
• Live Instruction Courses available
•Online and hybrid Courses available
The SkinStylus® Microneedling System is a unique fractional technology for doctors that offers exceptional results rivaling fractional laser resurfacing and chemical peels without the pain, downtime, and removal of precious skin layers, regardless of skin type. Check out our Before and After cases!
The EstheCeuticals® microneedling line is formulated for use with the SkinStylus® Microneedling System as well as after laser/IPL treatments. At SkinStylus®, we believe the foundation of a skin care regime that delivers results includes essential home care products designed as a system that is uncomplicated but highly effective. In order to beautify the skin, we have selected research supported active ingredients while avoiding ingredients that rely on unsupported marketing hype. Find out more about our revolutionary EstheCeuticals® products.
The SkinStylus®Microneedling System Professional Kit provides:
• Superior technology
• Cordless AND corded power options
• Topicals with active ingredients based on research, not hype
• The most comprehensive training available
ALL at a LOWER PRICE than any other comparable system!
We invite you to compare for yourself!
FDA COMPLIANCE: The SkinStylus® Microneedling Device is registered with the FDA as a Class 1 cleared device under 21 CFR 878.4820. FDA Class 1 devices are not required to pass 510(k) clearance and as such, are not required to be “approved”. However, FDA Class 1 devices are required to be registered. This means that both the importer and the manufacturer of the device must pay the FDA registration fee and register the firm and the device as well as list any importers. FDA indications for Class 1 devices under this section are: General Dermabrasion, Scar Revision, Acne Scar Revision, and Tattoo Removal. International and American physicians and those working under the direct supervision of a physician have submitted photos and data showcasing expanded functions of the device. Purchasers and users of the SkinStylus® Microneedling System are strongly urged to comply with any FDA indications and any state or local licensing restrictions for its use.