Clinical Study to Evaluate Different Energy-based Devices for Aesthetic Treatments.

Inclusion Criteria: * A healthy male or female 22 years of age or older. * Willing to undergo at least 1 treatment with the study device(s). * Understands and accepts obligation not to receive any other procedures in the treatment area through the length of the study. * Understands and accepts the obligation and is logistically able to be present for all visits. * Is willing to comply with all requirements of the study and sign the informed consent document Exclusion Criteria: * Is female and pregnant, has been pregnant within the last 3 months, is currently breast feeding or planning a pregnancy during the study period. * Takes or has taken oral isotretinoin, such as Accutane®, within the last six months. * Is using systemic steroids (e.g., prednisone, dexamethasone) prior to or during the course of treatment. * Is receiving or has received gold therapy. * Is taking medications that alter the wound-healing response or has a history of healing problems. * Has an active localized or systemic infection, or an open wound in area being treated. * Has a significant systemic illness, such as lupus, or an illness localized in area being treated. * Has a seizure disorders triggered by light. * Has a history of skin photosensitivity disorders. * Has a history of hypertrophic scars or keloid formation. * Has a history of radiation therapy in area to be treated. * Received fillers or neurotoxin injections in the treatment area within the past 2 weeks. * Has had a chemical or mechanical epilation within the last six weeks. * Currently enrolled in an investigational drug or device trial or has received an investigational drug or been treated with an investigational device within the area to be treated 6 months to entering this study. * Has any condition or is in a situation which in the investigator's opinion may put the subject at significant risk, may confound study results or may interfere significantly with the subject's participation. Radiofrequency Device Only: * Has a Pacemaker * Has any embedded electronic devices that give or receive a signal. * Has electronic implants, such as Implantable Cardiac Defibrillators (ICD) or Cardiac Resynchronization Therapy (CRT) devices: treatment may interfere with the functionality of the device and/or damage the electronic implant. * Is allergic to adhesives such as glues on medical tape: they should be alerted that a rash may occur on the neutral electronic monitoring pad (NEM or neutral pad) site, and an over-the-counter preparation may be used to treat the area. * Has nerve insensitivity to heat in the treatment area or in the neutral pad placement area. * Is allergic to topical anesthetic