Silhouette Soft® is a technological innovation that recontours the face, offering men and women what no treatment has ever provided in such a simple and minimally invasive way. Silhouette Soft® offers a reshaped face and restored volume by means of a treatment with minimal downtime at a physician’s office.
During your consultation, your physician will evaluate your expectations and review your medical history.
As there are some risks associated with all treatments, you need to fully disclose your medical history prior to treatment. Some skin allergies and neurological conditions, or medications can jeopardise your safety or results.
During the Treatment
Before conducting the treatment your physician will evaluate your needs and explain where the Silhouette Soft® sutures will be placed using a marking pen. The treated areas will be sterilised, and you may be given a topical anaesthetic to numb the area prior to the suture’s insertion.
Due to the sutures being inserted into the sub-cutaneous tissue there is relatively low level of discomfort during and after your treatment. Once the suture has been applied, the doctor performs slight compression of the tissue to reshape it by hand and to obtain the desired lifting effect. The non-inserted ends of the suture are cut off.
The number of sutures applied depends on the skin laxity and condition.
Following the Treatment
The insertion of Silhouette Soft®® elicits a minimal inflammatory reaction, this is normal and required. After placement patients may experience side some side effects, This may include minor pain, swelling and bruising.
The retightening effect is immediate : thanks to bi-directional cones distributed over the suspension suture that keep the skin in an elevated position. And the regenerative action is gradual : the main component of the suture (Polylactic acid: PLLA) during reabsorbtion stimulates the body so that it produces its own collagen. This action, which continues over time, restores the contours of the face and offers long term results.
Your physician will provide you with post-treatment recommendations and an aftercare programme to follow to ensure the best possible result.
Silhouette Soft® monofilaments are made of Polylactic Acid (PLLA) while the cones are made of poly (L-lactide-co-glycolide) (PLGA). They are two biocompatible polymers frequently used in medical devices for their outstanding tolerance in the body.
Silhouette Soft® is made in the USA and is subject to numerous sanitary controls. It has been developed after 6 years of research in permanent suspension sutures with cones used in plastic and reconstructive surgery.
With more than 150 000 treatments carried out so far, Silhouette Soft® has proven it’s safety and efficacy all over the world and is present in 70 countries.
It is CE marked device for the European market and the manufacturing site complies with the requirements of international standards ISO 13485.
Silhouette Soft® can be used to treat various parts of the face:
No special preparation is required prior to Silhouette Soft treatment. However, we recommend that you discuss your expectations and ask your doctor any questions you have before starting treatment. Inform the doctor of any treatment you have already received and of any medicines you are currently taking.
Like all procedures of this type there is a possibility of side effects, although not everybody experiences them. These side effects include infection, minimal acute inflammatory tissue reaction, pain, swelling and oedema. Transient brusing may also occur. Sometimes, a slight depression or skin irregularity may appear at the entry points. These inconveniences should disappear a few days after treatment.
If you experience any side effects, you should talk to your doctor.
Patients with foreign body sensitivity or known or suspected allergies to implant or instrument materials in particular plastic/biomaterial should not undergo the procedure. Do NOT use in patients with active sepsis or infection, active (or history of) autoimmune disease, patients under 18 years of age, pregnant or breastfeeding women, or patients with limited ability or un-willingness to follow post-treatment recommendations.
No, the treatment is performed under local anaesthetic, avoiding pain during insertion of the suture.
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