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.