Clinical Evaluation of Venus Versa Octipolar Applicator for Reduction of Abdomen Circumference

Exclusion Criteria

• •Pregnant or planning to become pregnant, having given birth less than 9 months ago, and/or breastfeeding.
• •Having any active electrical implant anywhere in the body,
• •Having a permanent implant in the treated areas
• •Having received treatment with laser, RF or other devices in the treated areas within 6 months of treatment or during the study.
• •Having undergone a liposuction surgery or any contouring treatment in the areas intended for treatment within 2 years of treatment
• •Having or undergoing any form of cancer
• •Suffering from significant concurrent illness, such as cardiac disorders, diabetes (type I or II), lupus, porphyria, or pertinent neurological disorders.
• •Having a anticoagulative or thromboembolic condition or taking anticoagulation medications
• •History of immunosuppression/immune deficiency disorders
• •Suffering from hormonal imbalance which may affect weight or cellulite
• •History of significant lymphatic drainage problems.
• •History of keloid scarring or of abnormal wound healing.
• •History of being especially prone to bruising.
• •History of epidermal or dermal disorders
• •Use of isotretinoin within 6 months
• •Significant change in diet or exercise regimen within a month of enrollment or during this study and/or weight loss or gain of 10 lbs (4.5 kgs) within 2 months of enrollment or during this study.
• •Participation in a study of another device or drug within 1 month prior to enrollment or during this study.
• •As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study.