Advin Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advin Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VINScreen Urine Drug Test Cup, ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card, ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card
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.
FDA 510(k) Regulatory Record - Advin Biotech, Inc.
3 devices