Silhouette Soft® is a minimally-invasive procedure that helps restoring volume to the mid-face and
offering women and men what no treatment has ever provided in such a simple and minimally invasive way: a reshaped face and restored volume by means of a 30-minute treatment at their doctor’s.*
Silhouette Soft® represents the state of the art suspension suture that opens up new treatment options for men and women.
48 years old
Mid face and Jaw Line
63 years old
Mid face and Jaw Line
48 years old
Mid face and Eyebrow
50 years old
Mid face
50 years old
Mid face
60 years old
Neck
45 years old
Mid face
56 years old
Mid face and Eyebrow
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:
Contours of the face
Jaw line
Cheeks and mid face area
Eyebrows
Neck
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.
Please select the option which best describes you.