FDA Device Establishments · JSON-LD · Markdown

CorneaGen

FEI 3005357288 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3005357288
Owner / OperatorCorneaGen (#10046718)
Address101 N Chestnut St Ste 303, Winston Salem, NC, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)OTZ
Regulation § (21 CFR)886.4300

External sources

Source: openFDA. Public-domain (CC0).