FDA Device Establishments · JSON-LD · Markdown

The Lotus Global Group, Inc.

FEI 3008776882 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3008776882
Owner / OperatorGlobalMed Technologies Co (#10051883)
Address1290 Jefferson St Ste C, Napa, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)GEX
Regulation § (21 CFR)878.4810
Proprietary namesOmnilux Revive & Blue

External sources

Source: openFDA. Public-domain (CC0).