# LIVEDO CORPORATION

FEI: 3005674561
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: LIVEDO CORPORATION (#9030441)

Address: Yodoyabashi Center Bldg. 8F-9F, 3-4-10, Koraibashi, CHUO KU OSAKA, 541-0043, JP

Mandatory US Agent: LIVEDO USA, INC.

## Products

Total registered: 1
Top product codes: EYQ
Regulation §: 876.5920

Proprietary names: Refre

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005674561%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005674561