Sa3, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sa3, LLC - FDA 510(k) Cleared Devices
Recent clearances: Silatrix Oral Gel, Silatrix Oral Gel
2
Total
2
Cleared
0
Denied
Sa3, LLC has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Latest FDA clearance: Oct 2025. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sa3, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eliquent Life Sciences, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sa3, LLC
2 devices