Spectrum Antimicrobials, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectrum Antimicrobials, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Spectricept Skin and Wound Cleanser
1
Total
1
Cleared
0
Denied
Spectrum Antimicrobials, Inc. has 1 FDA 510(k) cleared medical devices. Based in Petaluma, US.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Spectrum Antimicrobials, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dunn Regulatory Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Spectrum Antimicrobials, Inc.
1 devices