# IOX CO. LTD.

FEI: 3045824817
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: IOX Co. Ltd. (#10095982)

Address: 13-4 Nakano cho, Fukui City, 918-8185, JP

Mandatory US Agent: kapo optik

## Products

Total registered: 1
Top product codes: HOI
Regulation §: 886.5840


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223045824817%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3045824817