WEBEST Biotech,, LLC - FDA 510(k) Cleared Devices
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.
1 devices