Evolus Announces Submission of Premarket Approval Application to the U.S. Food and Drug Administration for Evolysse™ Sculpt Injectable Hyaluronic Acid Gel Product
NEWPORT BEACH, Calif.--(BUSINESS WIRE)--Evolus, Inc. (NASDAQ: EOLS), a performance beauty company with a focus on building an aesthetic portfolio of consumer brands, today announced that it has submitted the final module of its Premarket Approval (PMA) application to the U.S. Food and Drug Administration (FDA) for Evolysse™ Sculpt, an injectable hyaluronic acid (HA) gel product designed to restore mid-face volume. “This submission represents an important milestone in expanding our Evolysse™ col
Related Questions
What regulatory or competitive risks remain that could impact the approval or commercial rollout of Evolysse™ Sculpt?
How will the FDA decision timeline affect Evolus' (EOLS) near‑term stock price?
What is the projected market size and revenue contribution of Evolysse™ Sculpt relative to Evolus' existing product portfolio?