Sienna Biopharmaceuticals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sienna Biopharmaceuticals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SNA-001 Silver Photoparticle Topical Gel
1
Total
1
Cleared
0
Denied
Sienna Biopharmaceuticals, Inc. has 1 FDA 510(k) cleared medical devices. Based in Westlake Village, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sienna Biopharmaceuticals, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Sienna Biopharmaceuticals, Inc.
1 devices