Study of the MyoScience Tissue Remodeling Device for Facial Rejuvenation

Inclusion Criteria: * The subject must be a female 30 to 70 years of age. * The subject must have a clinical examination prior to treatment including assessment of hyperdynamic line severity. * The subject must have a wrinkle rating of at least "1" at rest in one or more of the following treatment areas (glabellar, lateral orbital, or frontalis). * The subject must have signed an informed consent form. * The subject should not have undergone any other facial cosmetic procedures at or above the level of the cheekbones within the past 6 months. * The subject should not be participating in any other facial cosmetic research study. Exclusion Criteria: * The subject is on a regular regimen of prescribed or over-the-counter anticoagulants. * The subject has an infection or skin problem at the injection site. * The subject has a history of facial nerve palsy. * The subject has marked facial asymmetry. * The subject has ptosis. * The subject has excessive dermatochalasis. * The subject has deep dermal scarring. * The subject has thick sebaceous skin. * The investigator is unable to substantially lessen facial lines by physical separation. * The subject has a history of neuromuscular disorder. * The subject has undergone prior surgery that alters the subcutaneous anatomy of the areas being treated. * Subjects with laxity of the canthal tendon and/or with lower lid retraction, and subjects who recruit their zygomaticus major muscle to animate their crow's feet. * The subject has any physical or psychiatric condition that in the investigator's opinion would warrant exclusion from the study or prevent the subject from completing the study.