FDA Device Establishments · JSON-LD · Markdown

Vitrolife Inc.

FEI 3003274090 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3003274090
Owner / OperatorVITROLIFE AB (#9037178)
Address3601 South Inca Street, Englewood, CO, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)MQL
Regulation § (21 CFR)884.6180
Proprietary namesG-IVF PLUS

External sources

Source: openFDA. Public-domain (CC0).