# Zimmer Biomet G.K.

FEI: 3012725451
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Zimmer Biomet APAC DFE (#10056128)

Address: 6-15 Shinmachi, Hiratsuka Kanagawa, 254-0076, JP

Mandatory US Agent: Zimmer Biomet

## Products

Total registered: 1
Top product codes: GDG
Regulation §: 878.4800

Proprietary names: HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012725451%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012725451