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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., August 20, 2025--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.

articleEvolus, Inc. Common StockAugust 20, 20255/company/evolus-inc/news/evolus-announces-submission-premarket-approval-120000075
Evolus Announces Submission of Premarket Approval Application to the U.S. Food and Drug Administration for Evolysse™ Sculpt Injectable Hyaluronic Acid Gel Product

About this update from Evolus, Inc. Common Stock

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More updates from Evolus, Inc. Common Stock

Evolus, Inc.SculptForward-Looking StatementsPremarket Approvalgel productdermal fillerstructured productregulatory approval