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Venus Concept is a leader in the global medical and aesthetic device market, pairing best-in-class technology with the first and only true subscription model in the industry.
Skin resurfacing continues to be one of the most sought-after treatments for people looking to improve the look and feel of their facial skin. This innovative medical aesthetic therapy has shown to be successful at treating a variety of skin concerns, including fine lines, wrinkles, acne scars, rosacea, stretch marks, enlarged pores, uneven texture, and other skin imperfections. Your patients have unique needs, and you want to be able to offer them the best skin resurfacing option for their skin goals. Below we’ll explore the difference between chemical peels and energy-based skin resurfacing treatments so you can give your patients the results they’re looking for.
During a chemical peel, a chemical solution is applied to the skin where treatment is desired and left on for a predetermined amount of time. The solution works to exfoliate and remove damaged skin cells, triggering the body’s healing response to generate healthy new skin cells. Chemical solutions of various strengths are available so that the peels can penetrate the skin to different depths depending on the cosmetic issues at hand—either the superficial layers, middle layers, or deeper in the dermis.
Because deeper peels reach further into the epidermis or even into the next layer, the dermis, they are able to address more advanced signs of aging, such as deeper wrinkles and extensive sun damage, or severe acne scars. However, while medium to deep peels produce dramatic results, they are more invasive treatments and therefore cause more pain and discomfort to the extent that anesthesia may be required during the treatment. They also incur an extended period of downtime as the skin heals.
Laser skin resurfacing can be broken down into two categories: ablative and non-ablative. Ablative lasers, such as the popular CO2 laser, remove several outer layers of skin to allow new skin to grow in its place. The process is intense, painful, and requires a long downtime and meticulous aftercare to protect the skin during the healing process. Today, most cosmetic professionals prefer fractionated lasers, which only remove a fraction of the skin in the treatment area. This allows the laser to safely penetrate into the deeper layers of skin to achieve more dramatic results with minimal downtime.
The latest in fractional laser resurfacing is Venus Concept’s NanoFractional RF™ (Radio Frequency) technology. A non-surgical solution to skin resurfacing, our NanoFractional RF™ energy works by delivering radio refrequency energy to the skin below the surface to encourage new collagen growth and help restore the skin’s natural firmness and tone. Because they are so much gentler on skin than their ablative counterparts, these treatments typically require little to no downtime while still delivering remarkable results.
Using NanoFractional Radio Frequency (RF) with SmartScan™ technology, Venus Viva™ MD is a fractional skin resurfacing system that allows complete control of ablation and coagulation for enhanced efficacy in resolving mild to severe skin damage. Because it is highly customizable, Venus Viva™ MD allows you to treat more patients and free up clinic space by replacing all other skin resurfacing devices with one lightweight, tabletop device.
Visit our Venus Viva™ MD page to learn more about the technology powering our cutting-edge skin resurfacing device and to view the amazing before-and-after photos from real patients.
Ready to bring NanoFractional RF™ skin resurfacing to your clinic? Contact us today to get started.
For more information call: (888) 907-0115 // info@venusconcept.com // 1880 N Commerce Parkway, Suite 2, Weston, FL, 33326 United States
REGULATORY CLEARANCES [ More ]
Venus Bliss™ is cleared by the FDA for non-invasive lipolysis of the abdomen and flanks in individuals with a Body Mass Index (BMI) of 30 or less, with the diode laser applicators. The (MP)2 applicator is cleared by the FDA for temporary reduction in the appearance of cellulite.
Venus Versa™ is cleared by the FDA as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators are cleared by the FDA for the treatment of benign pigmented epidermal and cutaneous lesions and treatment of benign cutaneous vascular lesions. The HR650/HR650XL and HR690/HR690XL applicators are cleared by the FDA for the removal of unwanted hair and to effect stable long-term or permanent hair reduction for Fitzpatrick skin types I-IV. The AC Dual applicator is cleared by the FDA for the treatment of acne vulgaris. The DiamondPolar™ and OctiPolar™ applicators on the Venus Versa™ system are cleared by the FDA for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The NanoFractional RF™ (Viva) applicator is cleared by the FDA for dermatological procedures requiring ablation and resurfacing of the skin.
ARTAS iX™ is cleared by the FDA with indication for use for harvesting hair follicles from the scalp in men diagnosed with androgenic alopecia (male pattern hair loss) who have black or brown straight hair. ARTAS iX™ is intended to assist physicians in identifying and extracting hair follicular units from the scalp during hair transplantation; creating recipient sites; and implanting harvested hair follicles.
NeoGraft® is cleared by the FDA with indication for use in suction-assisted follicular extraction and re-implantation. NeoGraft® is an auto-graft system and can be used on both male and female patients.
Venus Legacy™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides in females with Fitzpatrick skin types I-IV with the OctiPolar™ and DiamondPolar™ applicators, and temporary reduction in the appearance of cellulite with the 4D Body (LB2) and 4D Face (LF2) applicators.
Venus Velocity™ is cleared by the FDA for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae, for all Fitzpatrick skin types.
The Venus Viva™ MD is cleared by the FDA for the use in dermatological procedures requiring ablation and resurfacing of the skin, and the non-invasive treatment of moderate to severe facial wrinkles and rhytides for females in Fitzpatrick skin types I-IV with the DiamondPolar™ applicator.
Venus Freeze Plus™ is a non-invasive device cleared by the FDA for use in dermatologic and general surgical procedures for females for the treatment of moderate to severe facial wrinkles and rhytides in Fitzpatrick skin types I-IV, using the DiamondPolar™ and OctiPolar™ applicators.
Venus Heal™ is cleared by the FDA for the relief of minor muscle aches and pain, relief of muscle spasm, and temporary improvement of local blood circulation. The treatment of these conditions will lead to the treatment of certain soft tissue injuries and conditions.
Venus Glow™ is cleared by the FDA as a Class I motorized dermabrasion device. It provides a dermal rejuvenation treatment that works to open up and deep-clean pores. Venus Concept is the exclusive distributor for Venus Glow™.
Venus Epileve™ is cleared by the FDA for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs
re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types.
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