# Arthrex Japan G.K. (Shinjuku)

FEI: 3012470322
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: ARTHREX, INC. (#1220287)

Address: Shinjuku NS BLDG 28F, 2-4-1 Nishi-Shinjuku, Shinjuku-ku Tokyo, 1630828, JP

Mandatory US Agent: ARTHREX, INC.

## Products

Total registered: 2
Top product codes: HRS, HWC
Regulation §: 888.3030, 888.3040

Proprietary names: Arthrex Fracture Plates and Screws, Single/multiple component metallic bone fixation appliances and accessories

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012470322%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012470322