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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.
Treatment technology has come a long way since the first laser hair removal device was approved by the U.S. Food and Drug Administration (FDA) in 1997. Over time, researchers have been able to develop safer treatment options that minimize the risk of post-inflammatory hyperpigmentation (PIH) for patients with darker skin tones and offer greater operator control with spot size selection, pulse duration modes, built-in cooling technology, and more.
Today, the top developments in laser hair removal technologies have reduced the post-treatment hair regrowth rate by up to 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 hair follicles across a larger surface area, these developments in hair removal procedures reduce the risk of skin damage and improve treatment session times alongside patient comfort. Adjustable pulse width is a major factor in these developments.
One of four parameters that can improve the safety and effectiveness of laser hair removal treatments, pulse duration, which is also frequently called pulse width, refers to the time a device takes to deliver energy to a treatment area, or the time in which targeted tissue is exposed to laser energy. A key factor for determining optimal pulse duration for a particular treatment is thermal relaxation time (TRT).
TRT refers to the more specific amount of time in which it takes targeted tissue to release more than 50% of the heat delivered with each energy pulse. Because laser energy transfers to thermal heat once it penetrates the epidermis, the temperature of targeted tissue rises with each pulse. As energy disperses at the end of the pulse duration, the targeted tissue cools but some heat is retained. For treatments to be effective, thermal energy needs to be retained in the targeted tissue, rather than allowing it to disperse into surrounding tissue. To achieve this effect, pulse duration must be faster than TRT. Generally speaking, for larger areas, longer pulse durations are required for adequate heating of the targeted tissue, while shorter pulse durations will deliver the same effect to smaller treatment areas.
Pulse duration is also a key measurement for providers treating patients with a wider range of skin tones. Supporting greater efficacy and safety for prospective patients with darker and tanned skin tones, a longer pulse duration decreases the risk of damaging surrounding epidermis, including post-inflammatory hyperpigmentation (darkening of the skin) and hypopigmentation (lightening of the skin). Faster, shorter pulses, on the other hand, offer a more effective treatment for those with lighter skin tones while minimizing potential discomfort during treatment.
What truly sets the Venus Velocity™ diode laser hair removal device apart is the versatility to not only choose among three changeable tips with varying spot sizes—large at 7 cm2, medium at 3.51 cm2, and small at 1.69 cm2—but to also choose between two different pulse duration modes of operation: SLIDE and PULSE.
Unlike similar diode laser systems on the market that only offer a fixed pulsed or slide mode, Venus Velocity™ allows the operator to choose between the two options to better customize treatments to individual patient needs:
Having the unique ability to use either mode of operation provides unparalleled versatility for hair removal treatments. The repetition rate can also be adjusted to provide a tailored solution for your patient’s preferred treatment technique and comfort level.
Interested in learning more about Venus Velocity™’s advanced features and diode laser treatment technology? Contact an expert today using the button below.
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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