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Approximately one-third of all births in the United States are done using C-sections, and that rate is increasing every year as more women opt for this procedure. The abdominal surgical scar left by a C-section may be accompanied by pain, tenderness, rigidity, and itching. Furthermore, the appearance of the abdominal scar can be of a concern to some women.
Fortunately, there is a non-invasive solution that can produce satisfactory results on C-section scars without the downtime. As discussed by Dr. Kai O Kaye, board certified plastic surgeon and founder of Ocean Clinic in this clinical bulletin, he explores the option to treat abdominal scarring using the Venus Viva™ MD NanoFractional Radio Frequency (RF) device. He explains in detail the parameters and settings on this highly customizable skin resurfacing solution that were able to produce results like this:
As the radio frequency energy is produced by an electric current rather than a light source, it is not scattered by tissue or absorbed by melanin, making it possible for patients with Fitzpatrick skin types V and VI to benefit from treatment. Dr. Kaye trusts Venus Viva™ MD for its ease of use and the safety efficacy profile of the treatment. He is able to deliver exactly the amount of energy needed for a given scar by selecting voltage and pulse-width independently with the desired combination of ablation and coagulation. Topical numbing cream is typically used to manage any discomfort during treatment.
C-section scars are often thick and with strong adhesions to the underlying fascia, so the goal is to have an increased depth of energy delivered into the tissue to maximize ablation. Dr. Kaye generally works with a setpoint of parameters at 260-280 V and a pulse width at 25-28 ms. Depending on scar initial status and response, as well as skin type, 3-6 treatments are typically necessary to achieve the desired change in the C-section appearance.
Access this bulletin and see how you can leverage the customizability of Venus Viva™ MD to treat this common concern.
Click the download button below to read Dr. Kaye’s take on maximizing the efficacy of using ablation and resurfacing of the skin to treat C-section scars.
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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