# DENTAMERICA

FEI: 2024949
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: DENTAMERICA (#2024949)

Address: 18688 SAN JOSE AVE, City of Industry, CA, US



## Products

Total registered: 1
Top product codes: EKX
Regulation §: 872.4200


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%222024949%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=2024949