# THE ARGEN CORPORATION

FEI: 2433919
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: The Argen Corporation (#9021799)

Address: 5855 Oberlin Dr, SAN DIEGO, CA, US



## Products

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

Proprietary names: ArgenZ Ultra, ArgenZ Esthetic

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%222433919%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=2433919