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Recent studies have shown that people who have had COVID-19 and its variants are experiencing hair loss for months after recovering from the virus. This can understandably be a difficult experience for your patients, and when they turn to you for help it’s important to be ready with a solution. Here’s how you and your patients can navigate the complexities of COVID-related hair loss with the help of NeoGraft®.
According to the American Academy of Dermatology Association, the hair loss people are experiencing after having COVID-19 is fever-induced hair shedding. This is known as telogen effluvium and occurs when a fever interferes with the three stages of hair growth, causing more hair to enter the shedding phase at the same time. Most people will notice this happening two-three months after their illness.
For now, it appears that this shedding may be temporary, with the hair returning to normal growth in time. However, COVID-19 hair loss brings up an opportunity to open a discussion about hair loss with your patients. To dissuade further shedding and promote the hair to grow, here are a few at-home remedies they can try:
Scalp care: caring for the hair and scalp properly, by cleansing, exfoliating, and using gentle massage, can encourage new growth and less breakage where hair strands have been weakened from illness.
Honey: honey has a number of benefits for hair care, and using products that contain honey or applying a DIY hair mask can promote healthy hair.
Oils: dehydration is often a side effect of illness, and oils can be used to infuse the hair with moisture and protect it from further damage.
Hair masks: DIY hair masks and scalp scrubs incorporating honey, essential oils, and other ingredients can improve circulation in the scalp to encourage hair growth and improve the appearance of the hair.
If your patients are experiencing hair loss that is more severe, permanent, or continues long after they have COVID-19, then a hair restoration procedure is the answer. Venus Concept’s state-of-the-art NeoGraft® device uses the most advanced technology to perform hair restorations with precision, accuracy, and repeatability. The device takes the gold standard method of hair restoration, Follicular Unit Extraction (FUE), one step further with cutting-edge automation and robotics. The FUE technique is less invasive than the traditional strip method, resulting in a much faster recovery time for patients.
With NeoGraft®, the automated system supplants the need for linear grafts by extracting hair follicles in their natural groupings of 1-4 hairs. The highly specialized pneumatic arm then implants them in the area where more hair growth is desired. The newly implanted hair follicles continue the natural hair growth cycle and results improve each week, with full realization at 9-12 months post-procedure. The procedure is minimally invasive, less painful, leaves no linear scarring, and requires very little in terms of recovery or aftercare. Automation has made hair restoration faster and less expensive for providers and maximizes the consistency and quality of the transplanted graft for optimal follicular survival and growth. The transplanted hair will look natural, grow at the same rate as the surrounding hair, and should last for life.
For an example of the life-changing transformation a NeoGraft® procedure can have, we recently followed Jessi’s journey as she underwent a NeoGraft® hair restoration procedure. When she began to notice her hair thinning after having children, she turned to over the counter products and styling to cover it up. “I tried vitamins, shampoos, spray fibers—all of that stuff only helps the hair you have. It doesn’t grow new hair.” That’s when her friend recommended she looked into hair restoration, and she found out about NeoGraft®. As little as 18 months after the procedure, she booked her first salon appointment in ages. “Now that my hair is all grown, I feel like I can do any hairstyle. People are telling me how awesome and full my hair looks.”
Hair restoration is one of the most sought-after cosmetic procedures today. With each passing year, it proves itself as a solid offering for aesthetic clinics looking to maximize return on investment. The total market for hair restoration treatments has increased 16% since 2016 and it is now a $4.9 billion industry—there’s never been a better time to add hair restoration to your clinic offerings. When you offer hair restoration with a Venus Concept device, you also have the full support and backing of VERO Hair™, a comprehensive solution for growing your hair restoration business. It includes extensive post-sales support tools, including clinical training, marketing, and business development programs, giving you the competitive edge in the expanding hair restoration market. Speak to one of our experts today to see how we can support your success.
For more information call: (+62 21) 5890 1590 // info.id@venusconcept.com // Ruko Business Park Kebon Jeruk Blok B11 Jl. Meruya Ilir Raya No. 88 Kel. Meruya Utara, Kec. Kembangan West Jakarta 11620
REGULATORY CLEARANCES [ More ]
All devices have received Indonesian Health Ministry Approval for sale and use in Indonesia. (Izin Edar Alat Kesehatan)
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.
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 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 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 stretch marks at 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 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™.
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