View clinical trials related to Lax Skin.
Filter by:Open-label, non-randomized, prospective, multi-center, self-controlled clinical study with masked evaluation.
This is a prospective, multi-center, multi-phase, evaluator-blinded study of subjects undergoing a procedure with the Renuvion APR Device to improve the appearance of lax tissue in the neck and submental region.
All subjects will receive three, single-sided injections of PLLA, performed 1 month apart.