FDA Device Establishments · JSON-LD · Markdown

VEIN360

FEI 3015988948 · Reprocess Single-Use Device · Status: Active

FEI Number3015988948
Owner / OperatorVein360 (#10061626)
Address4460 Lake Forest Dr, STE 218, Blue Ash, OH, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)NUJ, GEI
Regulation § (21 CFR)878.4400

External sources

Source: openFDA. Public-domain (CC0).