Advin Biotech, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Advin Biotech, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Oct 2025. Active since 2019. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Advin Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LSI International, Inc. as regulatory consultant.
3 devices