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With age, the effects of a patient’s lifestyle or skin conditions become more emphasized, particularly so on the face. Cumulative sun exposure, a history of skin conditions, declining collagen production levels, unhealthy habits, long-term stress, and many more factors can contribute to a host of skin texture concerns, making skin resurfacing treatments a popular option.
The prospect of downtime and the risk of adverse effects like post-inflammatory hyperpigmentation (for those with darker skin tones) have been barriers for some patients in this past. Fortunately, great strides have been made in skin resurfacing technologies that allow patients to capture visibly improved skin tone and texture with little to no discomfort, no downtime, and less risk—beginning with customizable skin resurfacing treatments using Venus Viva™.
The Venus Viva™ skin resurfacing platform offers several features that allow greater operator control to deliver safe and effective treatment plans to a more diversified patient base and range of skin conditions.
Many skin resurfacing treatments are ablative, meaning they use some type of energy to evaporate tissue in order to create a controlled amount of damage in the skin. When skin is damaged, red blood cells bring oxygen and nutrients to the area to help it heal. Cells are also prompted to make collagen, creating a structure for new skin cells to form around.
When energy is applied in a fractional manner, it means there are tiny columns of energy applied through the skin that leave much of the surrounding tissue intact. The energy heats and evaporates tiny columns of the skin, creating micro-channels which appear to the naked eye like pin pricks. Natural healing responses then stimulate fibroblasts and rebuild an accumulation of collagen. The result is reduced skin damage and a more even-looking complexion, with low downtime.
The Venus Viva™ NanoFractional RF™ skin resurfacing system offers highly tunable power and pulse duration for greater operator control of ablation and coagulation.
Venus Viva™’s patented tip technology on the NanoFractional RF™ applicator features the largest spot size in the industry for faster coverage of the treatment area. Each applicator tip consists of 160 pins with a footprint of 38 µm2 each, arranged in groups of four. The pins gently penetrate the stratum corneum and a pulse of radio frequency is fired through the tip of each pin using SmartScan™ technology.
In the highly customizable MD Mode, the operator chooses the Joules and pulse duration, determining the level of ablation and coagulation that will be achieved in the target tissue. For example, a longer pulse duration with lower Joules will create less ablation and increase the amount of coagulation in the tissue, whereas decreased pulse duration and higher power (J) will create deeper ablation and less coagulation in the surrounding tissue.
When each group of four pins are activated, the other 156 pins serve as return electrodes. Current is switched between each group of electrodes for consistent energy deliver throughout the tip surface, with no return pads needed. The result is a safer treatment with more consistent clinical outcomes.
When combined with SmartScan™ technology, the patented tip offers a strong base with which to customize your patient’s treatments for reducing the appearance of acne and traumatic scars, striae, rosacea, dyschromia, deep wrinkles, rhytides, enlarged pores, and other uneven skin texture and pigmentation concerns for all skin types. (You can read more about treating stretch marks with the Venus Viva™ here.)
Venus Viva™’s NanoFractional RF™ applicator utilizes patented SmartScan™ technology, a unique algorithm that scans between randomized groups of pins to deliver energy at varying impact zone densities in one tip. This enables more uniform energy distribution over a treatment area and more effective skin resurfacing for diverse clientele. In particular, a lower energy density selection can lower the risk of post-inflammatory hyperpigmentation (PIH) for patients with darker skin tones.1
With pattern selection features and adjustable energy density and pulse duration, SmartScan™ provides flexibility that may require additional time and consumables in other skin resurfacing modalities. This all results in simpler, faster, and more cost-effective treatments that can enable a higher return on investment for you and a more comfortable and effective treatment for the patient.
Expand your clinic’s services with the DiamondPolar™ applicator for the treatment of moderate-to-severe wrinkles and rhytides. Using proprietary (MP)2 technology—a combination of Multi-Polar RF and Pulsed Electro Magnetic Fields (PEMF)—the Venus Viva™ device also features a DiamondPolar™ applicator that delivers multi-polar radio frequency to multiple tissue depths, enabling a faster ascension to therapeutic temperature and a comfortable patient experience.
The effects of Multi-Polar RF are enhanced by PEMF, a non-thermal energy emitted through the applicator’s electrodes that induces fibroblast proliferation through the release of the growth factor FGF-2.2 This growth factor helps with the remodeling of collagen and the creation of new capillaries. With new capillaries, blood supply is renewed and more nutrients are delivered to the treatment area for greater skin cell renewal.
The unique electrode placement of the DiamondPolar™ applicator allows for treatment around the eyes, along the jowls, and other smaller areas to firm up skin and smoothen fine lines and wrinkles. Treatments with this applicator are comfortable with no downtime, and RF technology is proven safe for all skin types. This applicator comes standard with every Venus Viva™ device.
Offering state-of-the-art technologies and easy-to-use features alongside two distinct applicators to treat a host of skin texture and tone concerns, the Venus Viva™ skin resurfacing system enables greater operator control over the delivery of your patient’s treatments, ensuring personalized treatments for your boutique medical aesthetics clinic as well as quick and effective solutions for the busy MediSpa.
Ready to customize your patient’s skin resurfacing treatments with your own Venus Viva™ system? Contact an expert today using the button below.
*Availability varies by region. Contact an expert to learn more.
For more information call: (888) 907-0115 // info@venusconcept.com // 235 Yorkland Blvd., Suite 900, Toronto, ON, M2J 4Y8 Canada
REGULATORY CLEARANCES [ More ]
Venus Bliss™ is cleared by the FDA and licensed by Health Canada 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, and licensed by Health Canada for temporary increase of skin tightening, temporary circumferential reduction, and temporary cellulite reduction. Venus Bliss™ has CE Mark as a non-invasive medical aesthetic device enabling a comprehensive approach leading to body contouring, addressing fat reduction, skin tightening, circumference reduction, and cellulite reduction.
Venus Versa™ is cleared by the FDA, licensed by Health Canada, and has CE Mark as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators are cleared by the FDA, licensed by Health Canada, and have CE Mark 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, licensed by Health Canada, and have CE Mark 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, licensed by Health Canada, and has CE Mark 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 DiamondPolar™ applicator is licensed by Health Canada and has CE Mark for non-invasive treatment of moderate to severe facial wrinkles and rhytides on females with Fitzpatrick skin types I-IV. The OctiPolar™ applicator on the Venus Versa™ system is licensed by Health Canada and has CE Mark for temporary body contouring via skin tightening, circumferential reduction, and cellulite reduction. The NanoFractional RF™ (Viva) applicator is cleared by the FDA, licensed by Health Canada, and has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin.
ARTAS iX™ is cleared by the FDA, licensed by Health Canada and has CE Mark 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, licensed by Health Canada and has CE Mark 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. It is licensed by Health Canada and has CE Mark for the temporary increase of skin tightening, temporary circumferential reduction, temporary cellulite reduction, and temporary wrinkle reduction.
Venus Velocity™ is cleared by the FDA, licensed by Health Canada and has CE Mark 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.
Venus Fiore™ received regulatory approval in Israel for aesthetic and functional treatment of the vagina, labia and mons pubis. Venus Fiore™ is available for sale in India, Hong Kong, and other selected Asian countries.
The Venus Viva™ MD is cleared by the FDA, licensed by Health Canada and has CE Mark for the use in dermatological procedures requiring ablation and resurfacing of the skin using the Viva™/Viva™ MD applicator, and the non-invasive treatment, reduction in the appearance of moderate to severe facial wrinkles and rhytides for females in Fitzpatrick skin types I-IV with the DiamondPolar™ applicator.
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 Epileve™ is cleared by FDA, licensed by Health Canada and has CE Mark 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. Venus Epileve™ is also CE-Marked for hirsutism.
Venus Freeze Plus™ 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. It is licensed by Health Canada for temporary skin tightening, and temporary reduction in the appearance of cellulite on the abdomen and flanks, using the DiamondPolar™ and OctiPolar™ applicators. The DiamondPolar™ applicator on Venus Freeze Plus™ has CE Mark for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and the increase of skin tightening, temporary circumferential reduction, and cellulite reduction with the OctiPolar™ applicator.
Venus Heal™ is licensed by Health Canada and can be used for the treatment of both acute and chronic disorders of the musculoskeletal system, such as muscle spasms, back pain, and soft tissue injuries, and results in effects such as pain relief, myorelaxation, increase of local blood circulation, and edema reduction. In the U.S., 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. These indications enable 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 Skin™ is a skin care line of various lotions and creams intended to improve different aspects of skin appearance, skin serums, and skin nourishment solutions.
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