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According to Dr. Richard Chaffoo, a board-certified plastic surgeon directing a hair transplant and restoration facility in San Diego County, women suffering from hair loss can benefit from “game changing” new technology.
While an increasing number of men are taking advantage of NeoGraft®, the latest innovation in hair restoration technology, San Diego triple board-certified plastic surgeon Dr. Richard Chaffoo says many women stand to benefit as well.
“Hair loss is more common for women than many people realize,” says Dr. Chaffoo, “and women with thinning hair may have greater motivation to seek treatment. Whereas men may view hair loss as aesthetically undesirable, in women, hair loss can have a devastating effect on self-esteem.”
The American Hair Loss Association says that women comprise about 40 percent of Americans living with hair loss (http://www.americanhairloss.org/women_hair_loss/introduction.asp).
Dr. Chaffoo’s La Jolla Hair Surgery Center is the only one of its kind in San Diego County – and one of only a handful nationwide – under the direction of a triple board-certified plastic surgeon. He and his staff specialize in NeoGraft for men and women, but Dr. Chaffoo speculates that he probably sees more female hair restoration clients than other providers. “It’s natural for a woman to seek out a plastic surgeon for her aesthetic concerns.” However, he encourages both male and female patients to choose a board-certified plastic surgeon for their procedures. “Plastic surgeons are uniquely qualified to perform every type of cosmetic surgery including hair replacement surgery,” he says.
Dr. Chaffoo’s hand-picked team of hair surgery professionals have many years of experience and training in all aspects of hair surgery. They are involved in the education and training of hair surgery professionals throughout the United States. “We attend national hair surgery meetings, both to learn and to teach. We take pride in remaining at the forefront of the field in hair replacement,” Dr. Chaffoo says.
Dr. Chaffoo and his team use a micro follicular unit extraction method assisted by the NeoGraft system. He characterizes this as revolutionary when compared to older approaches to hair transplant. The San Diego surgeon says “Simply put, we are using game-changing technology. I tell patients it’s like the invention of endoscopic surgery. The device, combined with our experience and training, produce a shorter and easier recovery without extensive scars.”
Instead of the “strip” method of hair transplant, Dr. Chaffoo utilizes an automated follicular unit extraction (FUE) technique that is comfortable, quick, and leaves no linear scars on the back of the head. His San Diego hair replacement clients have no sutures or staples, and no thinning of the hair at the donor site. “We are able to preserve a maximum amount of hair in case the patient wants a future hair surgery.”
Additionally, Dr. Chaffoo says that, with the assistance of NeoGraft, he is able to more gently harvest and handle the follicles, resulting in improved graft survival. That means more of the transferred hair will survive and thrive in its new location. This is a benefit for both women and men seeking to restore a fuller head of hair.
“Hair surgery is unique in aesthetic surgery in that the results are permanent,” Dr. Chaffoo says. “You may continue to lose existing hairs, but the transplanted hair will continue growing for life. It is a permanent investment in your appearance, and one best entrusted to a board-certified plastic surgeon.”
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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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