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.
Women’s bodies go through many changes over the years, brought about by childbirth, menopause, and aging. You may not realize it, but these changes can have a siginificant impact on your health, comfort, and overall quality of life.
There's no need to compromise—reclaim your life with treatments for your feminine health.
As we age, we experience changes in our feminine health that can affect the comfort, sensitivity, and even the external appearance of the vaginal area.
Vaginal atrophy is incredibly common: dryness and discomfort during intercourse affects 50% of postmenopausal women1, though it can occur at any age. Hormonal changes, trauma, aging, and other events can also cause affect vaginal laxity—a condition that over a third of women report along with symptoms of stress urinary incontinence, an overactive bladder, and a steep decline in the quality of their sex life, amongst other things2. These issues lead to decreased sensitivity and comfort during intercourse. In fact, 43% of women experience some form of sexual dysfunction3. As well, more and more women are seeking to rejuvenate the external appearance of their vaginal area and 43% of women consider the appearance of their labia minora important4.
Feminine health means taking care of what matters to you. Venus Fiore™ can improve the signs of unwanted feminine changes, and revitalize your gynecological comfort. Reclaim your life—renew your feminine comfort, confidence, and quality of life!
Everything you need to know about your feminine health treatment.
Radio frequency (RF) treatments are proven to be effective in encouraging the growth of new collagen and elastin, the building blocks of firm and healthy tissue. Venus Fiore™ uses a unique form of radio frequency in combination with Pulsed Electro Magnetic Fields, which is proven to enhance the restorative effects of RF by encouraging quick healing and improved blood circulation.
Venus Fiore™ offers three treatments using this combined technology: internal vaginal health restoration, labia skin tightening, and mons pubis reduction. Venus Fiore™ treatments use these technologies to help improve moisture levels, improve sensitivity, and increase elasticity.
Yes. Venus Fiore™ treatments use radio frequency technology, which is safe for patients of all skin types.
No, this treatment cannot be performed while you are pregnant. Please consult with a Venus Fiore™ treatment provider to determine the right time and treatment plan for you.
Please consult with your Venus Fiore™ treatment provider and discuss what type of surgery was performed to ensure that this procedure is right for you.
Yes. Each Venus Fiore™ treatment takes just 10-15 minutes per session.
One treatment usually takes just 10-15 minutes, and you can combine up to three treatments within one session.
Venus Fiore™ offers three treatments. You can opt for one, two, or all three treatments, one after the other, in one appointment. Each individual treatment requires 3-4 sessions, with effects lasting up to 6-12 months. Each treatment utilizes a single-use disposable tip for improved safety and hygiene.
Treatments are spaced 3-4 weeks apart. Consult your certified provider to get your own customized treatment plan.
Venus Fiore creates gentle heat in the vaginal canal in order to stimulate the production of new collagen which enhances moisture production and improves the firmness and elasticity of the tissue. The gentle heat is quite manageable due to the unique applicator design and temperature control features that ensure a very comfortable treatment experience.
You may experience a mild heat sensation both during and following the procedure. You may also have some erythema (or redness), which should resolve within a day.
There is no downtime, so you can resume your regular routine immediately afterwards.
The results will last approximately 6-12 months.
Everyone’s body is different. Please discuss your individual needs with your Venus Fiore™ treatment provider.
INDICATIONS FOR USE:
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.
REFERENCES:
1. Vaginal Atrophy. (n.d.). Retrieved from https://www.hormone.org/diseases-and-conditions/vaginal-atrophy.
2. Campbell, P., Krychman, M., Gray, T., Vickers, H., Money-Taylor, J., Li, W., & Radley, S. (2018). Self-Reported Vaginal Laxity-Prevalence, Impact, and Associated Symptoms in Women Attending a Urogynecology Clinic, The Journal of Sexual Medicine, 15(11), 1515-1517.
3. Schwarz, B., & Rivlin, M.E. (2019, August 12). Fast Five Quiz: Sexual Dysfunction. Retrieved from https://reference.medscape.com/viewarticle/916566.
4. Bouman, T.K., Koning, M., Van der Lei, B., Zeijlmans, I.A. (2009). Female Attitudes Regarding Labia Minora Appearance and Reduction With Consideration of Media Influence, Aesthetic Surgery Journal, 29(1), 65-71.
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For more information call: (888) 907-0115 // [email protected] // 235 Yorkland Blvd., Suite 900, Toronto, ON, M2J 4Y8 Canada
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, 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.
NeoGraft® is cleared by the FDA as a Class I device with motors and accessories intended for use as surgical instruments to cut hard and soft tissue. Venus Concept is the exclusive distributor for NeoGraft® in the U.S.
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 barba 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.
Venus Viva™ is cleared by the FDA, licensed by Health Canada, and has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin. The DiamondPolar™ applicator is licensed by Health Canada and has CE Mark for the treatment of moderate to severe wrinkles and rhytides in Fitzpatrick skin types I-IV.
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 stretch marks at the abdomen and flanks. 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 Freeze™ 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 stretch marks at the abdomen and flanks. The DiamondPolar™ applicator on Venus Freeze™ 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 Swan™ is cleared by the FDA for the non-invasive treatment of moderate to severe facial wrinkles and rhytides, and licensed by Health Canada for the non-invasive treatment of cellulite reduction, skin tightening, and temporary reduction in the appearance of stretch marks.
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