Sa3, LLC - FDA 510(k) Cleared Devices
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: General & Plastic Surgery.
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.
2 devices