# KEROX KFT.

FEI: 3009740550
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Kerox Kft. (#10041432)

Address: Kerox Utca 1, Soskut Pest, 2038, HU

Mandatory US Agent: mdi Consultants, Inc.

## Products

Total registered: 1
Top product codes: EIH
Regulation §: 872.6660

Proprietary names: Kerox Dental Zircostar, Kerox Dental Zircostar Zirconia Blank

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009740550%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009740550