# GLASSICO LTD.

FEI: 3008044481
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: Glassico Ltd. (#10030823)

Address: 23-162 Wadacho, Sabae Fukui, 916-0077, 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:%223008044481%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008044481