FDA Device Establishments · JSON-LD · Markdown

Vitrolife Inc.

FEI 3002757762 · Manufacture Medical Device · Status: Active

FEI Number3002757762
Owner / OperatorVITROLIFE AB (#9037178)
Address4940 Carroll Canyon Rd Ste 100, San Diego, CA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)CEP
Regulation § (21 CFR)862.1485
Proprietary namesOvuQuick One Step Ovulation Predictor Test

External sources

Source: openFDA. Public-domain (CC0).