# Zimmer Biomet Canada DFE

FEI: 3012392319
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: ZIMMER, INC. (#1822565)

Address: 2323 Argentia Road, Mississauga Ontario, L5N 5N3, CA

Mandatory US Agent: Zimmer Biomet

## Products

Total registered: 2
Top product codes: LPH, JDI
Regulation §: 888.3358, 888.3350

Proprietary names: LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012392319%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012392319