FDA Device Establishments · JSON-LD · Markdown

ANRIWELL

FEI 3043513123 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3043513123
Owner / OperatorAnriwell (#10095154)
Address2062 Business Center Dr Ste 125, Irvine, CA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)DXN
Regulation § (21 CFR)870.1130
Proprietary namesAW-301; Anriwell Pressia

External sources

Source: openFDA. Public-domain (CC0).