FDA Device Establishments · JSON-LD · Markdown

KEROX KFT.

FEI 3009740550 · Manufacture Medical Device · Status: Active

FEI Number3009740550
Owner / OperatorKerox Kft. (#10041432)
AddressKerox Utca 1, Soskut Pest, 2038, HU
Mandatory US Agentmdi Consultants, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EIH
Regulation § (21 CFR)872.6660
Proprietary namesKerox Dental Zircostar; Kerox Dental Zircostar Zirconia Blank

External sources

Source: openFDA. Public-domain (CC0).