WEBEST Biotech,, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
WEBEST Biotech,, LLC - FDA 510(k) Cleared Devices
Recent clearances: Webest Multi-Drug Urine Cup
1
Total
1
Cleared
0
Denied
WEBEST Biotech,, LLC has 1 FDA 510(k) cleared medical devices. Based in Irwindale, US.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by WEBEST Biotech,, LLC 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 - WEBEST Biotech,, LLC
1 devices