The Smartlipo Triplex 1440nm Wavelength Laser and the Sidelaze 800 Hand Piece for the Treatment of Facial Acne Scars

Inclusion Criteria: * A healthy male or female between 18 and 65 years old * Has unwanted facial acne scars and wishes to undergo laser treatments. * Is willing to consent to participate in the study. * Is willing to comply with all requirements of the study including being photographed, following post treatment care and attending follow up visits. Exclusion Criteria: * The subject is female and pregnant, has been pregnant within the last 3 months, is currently breast feeding or planning a pregnancy during the study period. * The subject is hypersensitive to light exposure OR takes photo sensitized medication. * The subject has active or localized systemic infections. * The subject has a coagulation disorder or is currently using anti-coagulation medication (including but not limited to the heavy use of aspirin) {greater than 81 mg per day}). * The subject is currently enrolled in an investigational drug or device trial, or has received an investigational drug or been treated with an investigational device within the planned treatment area 3 months prior to entering this study. * The subject has used Accutane within 6 months prior to enrollment. * The subject has the need to be exposed to artificial tanning devices or excessive sunlight during the trial. * The subject has had prior treatment with parenteral gold therapy (gold sodium thiomalate). * The subject has a history of keloids. * The subject has evidence of compromised wound healing. * The subject has a history of squamous cell carcinoma or melanoma. * The subject has a history of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or use of immunosuppressive medications. * The subject has an allergy to lidocaine and epinephrine. * The subject has any condition which, in the investigator's opinion, would make it unsafe for the subject to participate in this research study.