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Get your hair back by restoring a fuller hairline with the ARTAS® robotic hair restoration procedure. No stitches or staples are required, making your procedure virtually undetectable. Learn why ARTAS® is right for you!
The ARTAS® robotic hair restoration device is an advanced, minimally invasive hair transplant system that uses Artificial Intelligence (AI) technology to deliver precise, natural-looking results without leaving a linear scar. Using advanced image-guided robotics, ARTAS® can precisely analyze and dissect the best grafts from your donor area thousands of times per session, and then accurately identify where they should be implanted to achieve a seamless,
personalized hairline that’s perfectly suited to you.
The ARTAS® robotic hair transplant system starts by using 3D technology to help customize and plan your personalized hairline design. It then uses a high-definition stereoscopic vision system, robotic arm, and ARTAS Artificial Intelligence algorithms to identify and select the best hair follicles for transplanting. These follicles are then intelligently harvested with robotic precision and speed to preserve the natural look of your donor area, meaning no linear scarring. The ARTAS® procedure will also accurately identify and create an optimal recipient site and simultaneously implant the harvested hair follicles*. The minimally invasive process protects your existing healthy hair and maintains a natural appearance in both the donor area and the new implantation area.
NATURAL RESULTS: Noticeably thicker, natural-looking, and permanent hair growth starts around six months with continued growth over time.
MINIMALLY INVASIVE WITH NO LINEAR SCAR: The ARTAS® hair restoration system accurately and intelligently harvests and implants individual follicles without the use of scalpels, stitches, or staples, which means no unsightly linear scarring.
FAST AND EFFECTIVE: The robotic method enables greater precision and speed, making the procedure faster than other more manual hair transplant methods.
Everything you need to know about your ARTAS® treatment
Follicular Unit Extraction (FUE) is a minimally invasive hair transplant method that allows the removal of individual follicles from your donor area without a scalpel incision, and then implants them where you need more hair coverage
The ARTAS® system allows a minimally invasive procedure that is virtually undetectable. Unlike previous methods of hair restoration, there is no need for the surgical removal of a strip of scalp from the back and sides of the head. So, there is no linear scar after surgery, and no need for stitches or staples to close the wound. The benefit is a significantly shortened recovery time.
With the ARTAS® system, the FUE method can be done by getting a short trim. Trimming your hair in the donor area allows the ARTAS® system to accurately visualize, track, and harvest each grouping of hairs. You will receive detailed instructions from your doctor on the required length your hair needs to be before the procedure.
As part of the ARTAS® procedure, the scalp is locally anesthetized until numb. If you still feel any pain during the procedure, a physician will decide if it’s necessary to administer additional anesthesia to reduce discomfort. The patient typically feels no pain. Some patients can experience minor discomfort and swelling post-procedure, which subsides in one to three days.
Transplanted hair grows naturally in phases. New hairs are seen about three months after the procedure and will continue to increase over the course of a full year. At approximately six months, you will enjoy a noticeable improvement and after a full year, you will see full results. However, individual results and timelines may vary for each patient.
While hair loss may not necessarily stop after transplantation, the ARTAS® procedure uses your own permanent growing hair, typically from the back of your head, and your physician then implants this hair to the thinning areas of your scalp. As this hair might not be susceptible to the conditions that cause male pattern baldness, transplanted hair will typically last a lifetime. Your doctor will be able to assess your treatment options and discuss what you can expect.
For the procedure, the donor area will need to be shaved down with a zero guard in the harvesting area. As such, your treatment provider may advise you to cut your hair in preparation for shaving of the donor site at the start of your procedure. In addition to making this part of the process easier, cutting the hair short will also make for a less noticeable change after you return to your daily routine while the donor site heals and covers with new hair. For patients with longer hair, the donor area can be shaved in a way that it can be disguised by keeping the hair around it long to hide the shaved areas.
No. If your hair is long enough, the NeoGraft® procedure can be done by just shaving small areas,which can then be covered by the rest of your hair.
Depending on the number of grafts, the treatment can take anywhere from 4-10 hours. The number of treatments will depend on your unique circumstance, but in many cases, just one procedure can be enough to attain desirable results.
Your physician will numb the area with a local anesthesia before beginning the procedure, so you will likely feel minimal discomfort while the hair transplant is being done. Some physicians also offer the option of mild sedation for the duration of the procedure, depending on your preference. Once the numbing wears off and as the grafts heal, you may experience some tenderness around the donor site. This is a normal part of the healing process and should subside in a few days. Always be sure to consult with your physician with regards to post-procedure care and pain management.
No result can ever be guaranteed, but the before-and-after photos from previous NeoGraft® patients show that incredible results are very likely. With certified NeoGraft® providers, you can rest assured that you are in very good hands. Your physician will set as realistic expectations as possible and make sure all your questions are answered. For more real patient results, go to RealSelf.com, where NeoGraft® carries an average 96% “Worth It” rating from past patients.
There's typically very little pain or discomfort after the procedure. You may experience a slight amount of drainage for the first day after your procedure, but this is minimal. You must refrain from strenuous activity for two weeks, to ensure you do not cause any harm to the newly implanted grafts. You can expect the newly implanted grafts to be slightly raised in the first week after the procedure. Around three to four days later, they will start to scab over and then possibly shed. Shedding is good and a natural part of the healing process.
Recovery time after a NeoGraft® hair restoration procedure is much faster than traditional hair transplants, because there is no incision involved. The newly implanted grafts may feel tender and appear slightly raised at first, but this should subside in one week. You may also see some scabbing, but this should also flake off within a week. Your physician will instruct you on how to properly care for your new grafts, but most patients are able to return to their usual routine within two weeks after completing the procedure.
Immediately after your NeoGraft® procedure, the physician will ensure that the new grafts are secure and in their proper position. They will thoroughly rinse the treated areas and a light protective dressing may be applied. You will be given detailed instructions about how to care for the grafts when you go home, including any recommended shampoos, topical antiseptics, or hair care products. Because there is no incision, there is no need to get any sutures removed.
Extraordinary results speak for themselves
Improve thinning on the front of the scalp, as well as a receding hairline around the temples.
Devices that offer hair restoration: NeoGraft, ARTAS
Norwood Stage: 5
Results documented: 12 months after ARTAS®
Graft count: 1886 grafts
Courtesy of Bernstein Medical – Center For Hair Restoration, Robert M. Bernstein, MD
Improve thinning on the front of the scalp, as well as a receding hairline around the temples.
Devices that offer hair restoration: NeoGraft, ARTAS
Norwood Stage: 5
Results documented: 12 months after ARTAS®
Graft count: 1886 grafts
Courtesy of Bernstein Medical – Center For Hair Restoration, Robert M. Bernstein, MD
Improve thinning on the front of the scalp, as well as a receding hairline.
Devices that offer hair restoration: NeoGraft, ARTAS
Norwood Stage: 3A
Results documented: 9 months after ARTAS®
Graft count: 1066 grafts
Courtesy of the Hair Sciences Center of Colorado, James A.Harris, MD, FACS
INDICATIONS FOR USE:
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.
ARTAS® 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. It is also indicated for creating recipient sites for subsequent manual implantation of harvested follicles.
*Available on ARTAS® iX systems with the implantation feature
Click the button below to be directed to the dedicated NeoGraft® website, where you can search for a certified hair restoration provider in your area.
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 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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