TEL: (+62) 21 5890 1590
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.
Hair removal treatment technologies have drastically advanced since their humble beginnings in the 1960s and the latest intense pulsed light (IPL) and diode laser hair removal systems could be a valuable addition to your medical aesthetic clinic’s service offerings.
The ruby laser, developed by Theodore Maiman in 1960, was the very first laser aesthetic device designed for hair removal. While the technology worked to reduce hair growth, the process was tedious, and its side effects were numerous. Skin was frequently burned or damaged and even small areas were a challenge, with the device being able to target very few follicles at once.
By 1969, researchers were developing laser hair removal devices that target individual hair follicles and by 1970, the Food and Drug Administration (FDA) began to better study the efficacy of these devices. The laser technology in these devices wasn’t as strong as that found in the ruby laser, which led to less skin damage but also less effective targeting of hair follicles, meaning treatment plans could take years to offer adequate results. These early technologies were also mostly limited to patients with darker hair colors and lighter skin tones.
By the 1990s, FDA approval landed. The first approved laser hair removal device purportedly halted hair growth for up to three months but didn’t offer permanent hair reduction. During this time, researchers also began to explore the use of photosensitive carbon dyes in boosting the efficiency of laser hair removal devices and converting radiation into thermal energy for improved results. This led the way to safer options for patients with darker skin tones or lighter hair colors.
IPL-based medical aesthetic devices began to hit the market in the 1990s as well. With further technological developments over the last 20 years, IPL hair removal devices have gained traction due to their ability to treat larger areas in less time compared to previous hair removal procedures, as well as the capability to adjust emissions by using filters for increased accuracy by blocking certain wavelengths.
In 2008, the FDA approved the sale and marketing of in-home laser hair removal devices, with the very first approved device featuring a diode laser, which offers greater levels of control for a wider range of skin tones.
Today, laser hair removal technologies are able to reduce hair growth by 90-95%, with devices featuring diode laser technology that is safe for treating patients with darker skin tones and tanned skin. Delivering targeted heat through customized and controlled pulse rates and spot sizes to target individual hair follicles across a larger surface area, the most recent developments in hair removal procedures risk less damage to skin around the hair follicles (compared to older technologies with longer laser pulses, such as electrolysis) and quicker treatment sessions. Likewise, the addition of advanced cooling technologies makes these treatments much more comfortable for patients compared to earlier laser hair removal treatments and electrolysis.
As the popularity of hair removal procedures continues to rise, prospective patients may be tempted to save money by purchasing an at-home laser hair removal device. It’s important to convey to prospective patients that these devices can’t promise the same results as in-office alternatives, nor can they offer the level of safety a professional medical aesthetics clinic can provide. The results achieved using at-home devices certainly are not as long-lasting as those achieved using professional laser hair removal devices with the latest in IPL or diode laser technology, nor are they as effective on darker and tanned skin tones. For patients balking at the price point of a standard IPL or laser hair removal treatment plan, these points may be enough to convince them to invest in professional results and a more comfortable treatment that could save them money and time in the long run.
To learn more about our fast and effective hair removal systems featuring advanced IPL and diode laser technologies, contact us today.
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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