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The use of hair extensions has become commonplace. A popular option for fashioning a dramatic makeover in a hurry, we’ve become used to seeing them on celebrities at red carpet events and on social media. They’ve also been touted as a solution for masking thinning hair, patchiness, or bald spots for those experiencing hair loss. However, recently there has been a growing awareness that frequent use of hair extensions can result in damage to the scalp, the hair, and can even lead to permanent hair loss.
Made of either natural or synthetic fibers, hair extensions can be applied to the head in different methods, which vary in the degree of damage they can cause to the follicle. Temporary, clip-in extensions attach similarly to a barrette and are the safest option, causing minimal stress to the hair shaft. Semi-permanent extensions occasionally referred to as fusion extensions, require an adhesive and are glued to the hair close to the roots. These extensions typically last four to eight weeks. The most permanent of hair extension options is the sew-in weave, which requires the hair to be woven into tight braids so the extensions can be sewn with thread into the braid. These extensions will last for a long time, but they also put the most stress on the scalp, the roots of the hair, and the hair itself.
Hair extensions have come under increasing scrutiny lately for causing hair loss, with some trichologists (medical experts whose focus is hair) calling for a ban. While the occasional wearing of hair weaves and extensions should have minimal negative effects, people who resort to hair extensions regularly are prone to losing large patches of hair and experiencing thinning and damage that makes the strands break more easily. This is due to several factors and depends on the type of extensions used and the method of application. In some cases, the adhesives used to bond the extensions to the hair are liable to break the strands on removal. The added weight of hair extensions of any type can pull and stress the follicles. Most problematic is the sew-in method, which places tension on the follicles and scalp, causing the hair to fall out. This form of hair loss is called Traction Alopecia and can cause permanent damage to hair follicles and prevent hair regrowth.
Many people consider using hair extensions to cover up thinning hair without knowing that extensions can damage the hair further. With as many as 30 million women in the US alone report experiencing some sort of hair loss and the pressure to have red-carpet-worthy hair daily, it’s no surprise that hair extensions have become so popular. However, there’s a better solution available, one that improves the health of the scalp, and restores the look of a full head of hair, permanently.
If you have concerns about what’s involved in a surgical hair restoration procedure, don’t worry. Hair restoration treatment technology is highly advanced and designed to deliver natural results with minimal discomfort and almost no downtime. Here’s what to expect:
The treatment is safe: hair restoration procedures are performed by highly qualified physicians in a clinical setting with advanced medical equipment.
A natural look: AI technology selects the best placement for transplanted follicles to ensure a natural result, and the procedure leaves no linear scarring.
Minimal downtime: since the procedure is minimally invasive, the recovery time is quick, with most people returning to their normal activities in two weeks.
Satisfactory results: a 94% patient satisfaction rating says it all, but you can see the outstanding results for yourself at our before-and-after photo gallery.
In preparation for a hair restoration procedure, you and your provider will discuss your concerns and devise a plan to restore your hair to its full, healthy appearance. The procedure uses Follicular Unit Extraction, a safe and minimally invasive method for transplanting the hair follicles one at a time in the areas where more hair growth is desired. This allows for a more natural-looking result, without the linear scarring that previous methods might have entailed. The newly implanted hair follicles continue the hair growth cycle and can be cut and styled just like the rest of your hair. After a few months, the transplanted hair is indistinguishable from the surrounding hair, giving you back that full, healthy head of hair you’ve been missing.
To speak to one of our hair experts and begin your hair restoration journey today, use the search field below to find a clinic near you.
Find a certified Venus Treatments provider near you today who specializes in today’s top aesthetic medical solutions.
Search below to find a provider near you and to learn about our non-surgical aesthetic treatments with ARTAS®, NeoGraft®, Venus Bliss™, Venus Blilss MAX™, Venus Versa™, Venus Legacy™ Venus Versa™ Pro, Venus Velocity™, Venus Viva™ MD, and Venus Glow™.
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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.
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. It is an auto-graft system and can be used on both male and female patients.
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.
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.
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 cleared by the FDA, 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 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 Epileve™ is 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™ 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™ 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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