Discover these simple strategies that can help boost your aesthetic clinic’s day-to-day business operations for improved long-term revenue potential.
November 4, 2019
TEL: (888) 907-0115
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.
In the United States, Canada, and more westernized societies, studies suggest that acne breakouts are essentially a universal experience with 75–95% of adolescents experiencing some degree of acne vulgaris. In the U.S. alone, some 50 million people have acne at any one time. Part of the experience for most who suffer from acne is the struggle to control breakouts followed by the fear of scarring. Finding the right acne solution that results in clear, healthy skin can be a frustrating and draining process. It involves testing out different topical, prescription, or dietary solutions to see what just might work for them.
There is an opportunity in this area for aesthetics treatment providers to offer a comprehensive solution for acne patients. With just two applicators and the Venus Versa™ multi-treatment platform, paired with effective ongoing skin care, you can provide these prospective patients with a holistic acne treatment plan that reduces acne-related redness and inflammation, kills acne bacteria to prevent future breakouts, and minimizes the appearance of existing acne scarring for a brighter, clearer, healthier-looking complexion.
Using the AC Dual applicator equipped with Intense Pulsed Light (IPL) technology, Venus Versa™ acne reduction treatments utilize a dual-wavelength approach to target acne-causing bacteria while promoting the healing of breakouts. Blue light targets porphyrins—organic compounds that are produced by P. Acnesbacteria—destroying the bacteria to prevent future breakouts. Red light, delivered in a longer wavelength, penetrates deeper into the skin and targets dilated blood vessels and oxyhemoglobin, reducing inflammation and likely allowing faster recovery of the sebaceous glands . Furthermore, the applicator features a built-in real-time cooling system that monitors temperature 1,000 times/second to better ensure patient safety and comfort. Typically, traditional acne treatments focus on just one of two aspects—treating the cause or reducing the visible symptoms. Venus Versa™’s dual approach cuts down on treatment steps for patients and delivers effective results with just one treatment plan. Additionally, treatment sessions typically last from 15 to 20 minutes, making this option even more attractive to your prospective patients with busy schedules who are seeking a simple solution that works.
When equipped with the NanoFractional Radio Frequency (RF) with SmartScan applicator, Venus Versa™ offers a non-invasive fractional ablation system that harnesses the power of radio frequency (RF) technology to resurface the skin, improving the appearance of acne scars and other signs of uneven skin texture for smoother, more even-toned skin. The applicator tip features a spot size that is one of the largest in the industry and treatments require no anesthesia, making quicker work of treatment sessions to allow for a smoother schedule—a key factor for improved patient retention. SmartScan technology uniquely distributes energy across a small footprint per pin and at variable energy densities to ensure sufficient tissue is left intact between each microdermal wound. This promotes faster healing, minimal downtime, lower occurrence of PIH, and greater patient comfort. When used to follow up an acne reduction treatment plan, the result is a comprehensive, fully customizable plan that ensures your patients can keep up with their busy lives without having to put their aesthetic goals on the backburner.
It is advised that patients are made aware that some maintenance treatments may be required to ensure long-term skin health. However, you might also consider additional options that can better support the patient’s skin care while establishing a more loyal aesthetics client base. For patients whose acne may be a result of excess sebum production, regular Venus Glow™ dermal rejuvenation treatments may help. Venus Glow™ treatments utilize a powerful tri-modality approach to deep-clean pores. This helps to reduce bacteria buildup and control sebum secretion, so patients may better maintain their noticeably healthier, natural glow with less worry regarding the return of acne breakouts. Venus Glow™ treatments also help to restore skin hydration while increasing local micro-blood circulation to help boost skin’s natural collagen and elastin production levels, which can help to complement results from some of your clinic’s other aesthetics treatments.
Interested in learning more about how you can expand your acne treatment services with Venus Versa™ and Venus Glow™? Contact an expert today using the link below to get started.
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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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