A dissatisfied patient could ruin your hair restoration business. Avoid the damage with a thorough patient evaluation and selection process.
March 5, 2020
TEL: (888) 907-0115
Venus Concept is a leader in the global medical and aesthetic device market, pairing best-in-class technology with the first and only true subscription model in the industry.
Medical aesthetics have come a long way in recent years. The procedures and results of yesteryear are a far cry from what is possible today, particularly with the significant advancements in robotics and artificial intelligence (AI) in the medical and aesthetic fields. So far, natural-looking, effective results for hair transplantation procedures are well-proven with robotic and AI technologies. But what you’re likely wondering is: how can a robotic and AI-assisted hair restoration system, such as ARTAS iX™, benefit your medical aesthetics business?
With 1.2 billion men experiencing some form of hair loss around the globe and with the hair restoration market expected to surpass the $31 billion value mark by 2025, there are certainly lucrative business opportunities in the field. Of these 1.2 billion men experiencing hair loss, 29 million are seeking a solution and 9.7 million are looking to the ARTAS iX™ procedure. What is piquing their interest? Advanced technology and natural-looking results that are further customized and optimized with the assistance of the ARTAS iX™ robotic and AI technologies.
ARTAS iX™ is a proprietary, patented, and FDA-cleared robotic hair restoration system that looks quite impressive to today’s tech-interested patients—but this demand is just the beginning of the key benefits this system offers. Featuring advanced AI capabilities/algorithms, an advanced multi-camera stereoscopic vision system with 44-micron resolution, and a 7-axis Kuka robotic arm, ARTAS iX™ delivers unmatched intelligence, precision, repeatability, and clinical efficiency.
Advanced technological features, including robotics and AI technology, make the ARTAS iX™ system a significant advantage to your medical aesthetics clinic, especially if you are an experienced hair restoration surgeon and would like to distinguish your practice as the top-tier provider (OR elevate your practice to the next level).
The unique ARTAS iX™ harvesting system uses advanced image-guided robotics that precisely dissect follicular units thousands of times per session using intuitive controls and intelligent algorithms that select and harvest the patient’s donor hair for transplant. The 7-axis arm offers dexterity and ease of movement with 0.1mm repeatability for the most effective angles for analyzing, extracting, and implanting follicles. With force and torque sensors in each joint, operators like yourself are able to monitor the machine and control these metrics for a more customized treatment for your patients that does not sacrifice precision for comfort. The ARTAS iX™ device allows you to collaborate with robotics and AI technology to achieve safe, effective, and customized outcomes every time.
The ARTAS iX™ system’s AI technology records patterns and adjustments you’ve made in past procedures to continuously learn and improve for a more streamlined treatment with each procedure. The system’s field of vision is capable of monitoring the position and orientation of hairs at a speed of 60 times per second, while recognizing and identifying key features and adjusting for patient movement. Finally, simultaneous and intelligent recipient site-making and implantation creates procedural efficiencies, while reducing trauma to hair follicles and surrounding tissue for optimal outcomes.
With the help of AI technology, the ARTAS iX™ system is able to intelligently analyze and select appropriate grafts from the donor area without the risk of linear scarring or over-harvesting. It also intelligently implants donor follicles in a pattern, density, and angle for optimal distribution while preventing trauma. This ensures the most natural-looking results while minimizing the likelihood of errors that could risk negative results. With machine learning on the device, outcomes are consistent, and robotics-assisted harvesting and implantation offers a high yield of usable follicles for a natural-looking appearance in both the donor site and the implantation area.
In all, the ARTAS iX™ robotic hair restoration system offers five key benefits for you, the operator, and your medical aesthetics clinic:
Ready to add an ARTAS iX™ robotic hair restoration system to your clinic today? Contact an expert using the button below to get started.
For more information call: (888) 907-0115 // info@venusconcept.com // 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.
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.
Copyright 2023 Venus Concept. All rights reserved.
You are entering our website. For other countries/regions and language options, please click the SELECT A DIFFERENT REGION button below.
SELECT A DIFFERENT REGIONAre you looking to get a treatment? Please visit our patient website to learn more.
Click HereBe aware of schemes involving fraudulent job postings.
Read More