Sienna Biopharmaceuticals Files 510(k) Submission with FDA for SNA-001, its Novel Silver Photoparticle Technology to Remove Light Hair
SIENNA BIOPHARMACEUTICALS (SNNA)
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Source: GlobeNewswire
WESTLAKE VILLAGE, Calif., Oct. 07, 2019 (GLOBE NEWSWIRE) -- Sienna Biopharmaceuticals, Inc. (Nasdaq:SNNA), a clinical-stage biopharmaceutical company, today announced that the Company has filed a Premarket Notification 510(k) submission to the U.S. Food and Drug Administration (FDA) for SNA-001, a topical pre-treatment to standard laser devices to remove unwanted light hair, and has received acknowledgement from FDA that the submission has been accepted. The purpose of the 510(k) notification is to allow for commercial use of SNA-001, in conjunction with a 810 nm Diode laser, for the removal of unwanted white, gray, blonde, light red and light brown hair in women or men. Available for nearly 25 years, laser hair removal is one of the most commonly performed aesthetic procedures in the world. With more than 12 million laser hair procedures performed annually in the United States1, countless patients have benefitted from the lasting results of laser hair removal, except for those
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