# KERAMED INC.

FEI: 3012483804
Status: Active
Establishment types: Manufacture Device in the United States for Export Only
Owner/operator: KeraMed, Inc. (#10030689)

Address: 710 Dunn Way, Placentia, CA, US



## Products

Total registered: 1
Top product codes: HQM
Regulation §: 886.3400

Proprietary names: KeraKlear Artificial Cornea

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012483804%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012483804