Sonoma Pharmaceuticals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonoma Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Microdacyn Hydrogel, Microdacyn Wound Care Solution, Microcyn Antimicrobial Hydrogel
6
Total
6
Cleared
0
Denied
Sonoma Pharmaceuticals, Inc. has 6 FDA 510(k) cleared medical devices. Based in Petaluma, US.
Latest FDA clearance: Jun 2026. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sonoma Pharmaceuticals, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sonoma Pharmaceuticals, Inc.
6 devices
Cleared
Jun 24, 2026
Microdacyn Wound Irrigation Solution
General & Plastic Surgery
86d
Cleared
Nov 08, 2024
Microdacyn Hydrogel
General & Plastic Surgery
260d
Cleared
Sep 13, 2024
Microdacyn Wound Care Solution
General & Plastic Surgery
345d
Cleared
Apr 02, 2018
Microcyn Antimicrobial Hydrogel
General & Plastic Surgery
101d
Cleared
Dec 01, 2017
Alevicyn SG Antimicrobial Gel
General & Plastic Surgery
156d
Cleared
Nov 15, 2017
Microcyn Plus Antimicrobial Wound Care Solution
General & Plastic Surgery
56d