FDA Device Establishments · JSON-LD · Markdown

KERAMED INC.

FEI 3012483804 · Manufacture Device in the United States for Export Only · Status: Active

FEI Number3012483804
Owner / OperatorKeraMed, Inc. (#10030689)
Address710 Dunn Way, Placentia, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HQM
Regulation § (21 CFR)886.3400
Proprietary namesKeraKlear Artificial Cornea

External sources

Source: openFDA. Public-domain (CC0).