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Hair procedures have come a long way since our grandparents’ day. Over just a few decades, hair transplantation technology has dramatically evolved to become a minimally invasive procedure that requires less downtime and improved comfort compared to earlier procedures while achieving compelling, natural-looking results. But exactly how far has it all come? How do today’s top hair restoration procedures compare to those of the past?
According to the International Society of Hair Restoration Surgery, and most accounts today, the traditional hair transplant procedure dates back to the 1930s. While Dr. Norman Orentreich has often been dubbed the father of hair transplantation, Dr. Shoji Okuda has more recently been attributed with the development of the punch graft hair transplant procedure, as proven in The Okuda Papers. In the 1930s, Dr. Okuda established the procedures to help burn victims restore their hair growth. However, with the beginning of World War II, Okuda’s research and work did not make it outside of Japan until 2004, when The Okuda Papers were located and translated to English.
In North America, Dr. Norman Orentreich is credited with establishing the beginning of a revolution in aesthetics and the beginning of hair transplantation procedures. More specifically, in 1952, Orentreich performed the first known transplantation for the treatment of male pattern baldness. Initially, Orentreich’s findings were not widely accepted until his landmark study was published seven years later. In this paper, Orentriech pioneered the donor-dominance concept that proved hair follicles on the back and sides of the head are often more resistant to balding and will sustain healthy growth when harvested and implanted in areas that follicles have become dormant or damaged.
Unfortunately, Orentreich’s method required large circular skin grafts, equivalent to the size of pencil erasers, to be harvested and transplanted. Think of it like a cut and paste function. Often, the results looked unnatural or, as the Wall Street Journal described it, the procedure resulted in a “toothbrush” type look, with circular sections of hair compared to the rows of bristles on a brush. Nevertheless, the popularity of the procedure grew into the 1970s. Being the only surgical hair transplantation option at the time, those wanting a more impactful hair restoration solution didn’t have much of a choice.
From the 1980s to the 2000s, strip harvesting—also known as follicular unit transplantation (FUT)—replaced hair plugs as the industry’s gold standard. Using the FUT technique, physicians harvest a strip of skin from the back of the scalp. For optimal results, the physician carefully plans these cuts to ensure intact and healthy hair follicles will be removed. The area from which the strip is taken is then stitched closed while the physician’s assistants separate naturally formed groupings of hair follicles (follicular units) from the harvested strips. In the process, excess tissue is removed as much as possible without damaging the follicles. The physician then creates micro-puncture sites for transplanting the grafts with follicles placed in a predetermined arrangement to better match the patient’s natural hair density and growth patterns.
While the results of strip harvesting may appear more natural than hair plugs, the procedure results in linear scarring in the donor area. Downtime is shortened to approximately two weeks, but patients may have to wear their hair long enough to cover any potential scarring and stitches.
Improving upon the FUT method, follicular unit excision (FUE) harvesting first came about in Japan in 1988 but didn’t take hold in the hair restoration industry because the method required extensive time and costs to learn, and the technology had not yet been developed to support physicians in this process. With time, it saw progress with FUE procedures now the gold standard in hair transplantation.
Using the FUE technique, individual follicular units of one to four hairs are excised using simple local anesthesia with micro-punches no more than one millimeter in diameter. The physician then creates suitable micro-puncture sites to transplant the grafts based on the density and pattern of the patient’s hair growth. Because FUE uses small, circular incisions to separate the follicular unit from its surrounding tissue, tiny holes are left in the scalp in donor sites that don’t require stitches and naturally heal in just a few days with no risk of linear scarring. Patients of FUE hair restoration procedures may expect up to a week of downtime with minimal pain and discomfort expected, though you can explore more of what to expect during an FUE procedure here.
While the first hair restoration procedures using the FUE technique took a substantial time to complete and required a steady hand—physician fatigue was certainly a risk during a procedure—new technology has allowed for greater patient comfort, safety, accuracy, and optimal results. To begin, unlike the more traditional harvesting methods by hand, the NeoGraft® FUE hair restoration procedure skips the scalpel for an automated handpiece that features advanced technology to gently incise and remove donor follicles, resulting in little to no patient discomfort during the procedure. Using the device, physicians are better able to sort and implant hair follicles at an angle and in a pattern that offers more natural-looking outcomes in less treatment time.
More recently, robotics have also entered the mix with the ARTAS iX™ robotic hair restoration device. In particular, the ARTAS iX™ utilizes the FUE technique alongside Artificial Intelligence (AI) technology to deliver precise, natural-looking results. The ARTAS iX™ system starts by tapping into 3D technology to help your physician customize and plan your personalized hairline design based on your own hair growth and density patterns. Using a high-definition stereoscopic vision system, robotic arm, and ARTAS Artificial Intelligence™ algorithms, your physician can use the ARTAS iX™ system to identify and select the best hair follicles for transplanting while flagging low hair density areas and blocking them out from harvesting, reducing the risk of over-harvesting. Selected donor follicles are then intelligently harvested with robotic precision and speed to preserve the natural look of your donor area. Using 3D technology and your customized hairline design, the physician can then tap into the ARTAS iX™ system’s advanced technology to accurately identify and create optimal recipient sites while simultaneously implanting the harvested hair follicles. In all, existing healthy hair is protected, and a natural appearance remains in both the donor and implantation areas. The system’s robotic method enables precision and speed for a faster procedure than more manual FUE methods.
Interested in learning if you’re an ideal candidate for an ARTAS iX™ or NeoGraft® FUE hair restoration procedure? Locate an expert near you to learn more about the technology, the technique, and a customized hair restoration treatment plan that’s right for you.
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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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