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Author: Sudeep Roy, M.D.
The hair transplant procedure was developed from a very simple observation: hair on the back and sides of the head is resistant to the effects of hormonal loss classically seen in male and female pattern baldness. This is called donor dominance. Transplanting these hairs to areas of loss on the scalp produces long-lasting, new growth of hair that is shielded from further shedding.
How the transplant is actually performed has evolved quite a bit over the years. Two major techniques exist, follicular unit transplantation (FUT also known as the “strip procedure”) and follicular unit extraction (FUE). Although still useful and appropriate in certain cases, FUT is being performed less and less due to increased recovery time, the need for suture removal and the possibility of unattractive, linear scarring. NeoGraft® is at the forefront of manual FUE, whereby naturally occurring groups of hair follicles (follicular units) are extracted or harvested through an automated punch-like device and then implanted in areas of hair loss. The punches are less than 1mm in diameter, ensuring an appropriate protective cuff of tissue around the harvested grafts while preventing visible scarring.
There are three main reasons that set NeoGraft® apart from all other manual extraction devices: 1) The most ergonomic handpiece available on the market allowing comfortable, precise and efficient extraction of follicular units which saves patients time and improves graft yield; 2) Rapid extraction and preservation of harvested grafts into a dedicated collection chamber on the handpiece itself that keeps the grafts moisturized and healthy while they await implantation and 3) NeoGraft® hair technicians, affectionately known as the VeroGrafters™, are the most experienced and highly-trained FUE hair techs in the country, ensuring the best possible outcome for every procedure alongside the physician.
The procedure has three fundamental steps. 1) Harvesting, 2) Recipient site create and 3) Implantation of grafts. The only discomfort felt during the procedure is when the scalp is anesthetized with local anesthetic to ensure a comfortable and painless treatment session. In our office, we routinely administer oral sedation to help patients with any pain and anxiety experienced by the patient as well as nitrous gas (laughing gas similar to that available in a dentist’s office) to maximize patient relaxation through the numbing process. Depending on the number of grafts planned for the procedure, the procedure can last anywhere between 2-8 hours. Patients often watch their favorite shows or catch up on work emails during the recipient site creation and implantation stages! Unlike robotic hair transplantation, only the donor area at the back of the head needs to be shaved down for the procedure allowing for a more seamless transition to everyday life after the procedure, and there is no need to strap the head down to the treatment chair for immobilization, which can certainly add to patient anxiety.
At Roy Facial Plastics, every patient receives Platelet-rich plasma (PRP) injections to the scalp (harvested from the patient at the start of the procedure and rich in growth factors) to enhance their transplant results, which has been scientifically proven to shorten the expected shedding period post-procedure, reduce the overall amount of shedding post-procedure and improve graft survival and growth.
Once the procedure is over, a head dressing is applied to protect the donor and recipient sites for the first two days. Once this is removed, the hair can be gently washed although normal showering should only be resumed after 10 days. Social recovery is approximately 7 days, and the donor site typically heals up completely by 10-14 days. Physical activity should be limited for 7-14 days to expedite recovery. The new hair grafts will undergo a new hair cycle and growth will start to be noted by 6-12 weeks and continue steadily thereafter. By 8-10 months, your final result will be apparent and you can enjoy your own hair, naturally.
Good candidates are those who:
Maximize your chances for a successful hair restoration by working with a highly qualified, experienced team that will be readily available to you through every step of the procedure and beyond. Even if you are simply contemplating options for your hair loss and not necessarily ready to undergo a hair transplant, it is worth meeting a hair restoration specialist to educate yourself on the various options available, including topical and medical therapies.
I wish our readers the best as you explore hair restoration treatments. Do not hesitate to contact us with questions or consultation inquiries!
Disclaimer: The content within this site is not intended to provide diagnosis, treatment or specific medical advice. The products and claims made about specific products and treatments through this article have not been evaluated by the United States Food and Drug Administration and are not approved to diagnose, treat, cure or prevent disease. Please consult with a NeoGraft® Certified Physician or other healthcare professionals regarding any medical or health-related diagnosis.
Sudeep Roy, M.D. is a fellowship-trained facial plastic surgeon certified by the American Board of Otolaryngology – Head and Neck Surgery, who practices in Glenview and Chicago, Illinois. He is a member of the American Academy of Facial Plastic and Reconstructive Surgery (AAFPRS) and the Midwest Association of Plastic Surgeons. He received a Bachelor of Science degree from Stanford University in Palo Alto, California and a Doctorate of Medicine from New York Medical College in Valhalla, New York, graduating with top honors. He was elected to the Alpha Omega Alpha National Medical Honors Society, reserved for medical students all around the country with the highest academic achievements who also exhibit good character, leadership, professionalism and a dedication to community service. After medical school, he moved to Philadelphia to complete a five-year, rigorous surgical training program in Otolaryngology – Head & Neck Surgery at Thomas Jefferson University Hospital, ranked in the top ten hospitals (US News & World Report 2017) for the specialty. Having a unique eye and skill for facial aesthetics and reconstructive surgery, Dr. Roy went on to pursue advanced training in Facial Plastic and Reconstructive Surgery in Austin, Texas with renown facial plastic surgeon, Edward D. Buckingham (Buckingham Center for Facial Plastic Surgery).
Dr. Roy is proud to have started his own practice in Glenview and Chicago, Illinois offering his patients concierge service for a variety of facial plastic surgical procedures including follicular unit extraction hair restoration. He is certified in both robotic and manual follicular unit extraction as well as follicular unit transplantation (“strip” harvesting). Now, with NeoGraft® 2.0 in his arsenal, Dr. Roy is at the forefront of technological advancement in manual follicular unit extraction to achieve the best possible outcomes for his patients.
Interested in learning more about how a NeoGraft® partnership can benefit your practice? Contact an expert today at the button below.
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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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