FDA Device Establishments · JSON-LD · Markdown

GUANGZHOU WONDFO BIOTECH CO., LTD.

FEI 3023322455 · Manufacture Medical Device · Status: Active

FEI Number3023322455
Owner / OperatorGUANGZHOU WONDFO BIOTECH CO., LTD. (#9064561)
AddressBuilding 1, No.2 Huangqi Street, Songshan Lake Park, Dongguan Guangdong, 523787, CN
Mandatory US AgentLSI International Inc.
Registration expiry2026
Initial importer flagN
Registered products11
Product codes (top 20)QBF, NGL, NFT, LCM, PTH, NGG, NFW, NFY, NFV, QAW, PTG
Regulation § (21 CFR)862.3700, 862.3650, 862.3100, 862.3150, 862.3610, 862.3870, 862.3250, 862.3170, 862.3910, 862.3620
Proprietary namesPRIME SCREEN® Single Panel Urine Test Cannabinoids (THC20); SAFElife™ T-Dip Multi-Drug Urine Test Panel Dx

External sources

Source: openFDA. Public-domain (CC0).