# VIVATEC CO.,LTD.

FEI: 3025032529
Status: Active
Establishment types: Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: VIVATEC Co.,Ltd. (#10092839)

Address: 2-10-1,Kitahanada-cho,Kita-ku,, Sakai-shi Osaka, 591-8002, JP

Mandatory US Agent: Frederick Hart Co., Inc.

## Products

Total registered: 1
Top product codes: EFW
Regulation §: 872.6855

Proprietary names: TOOTHBRUSH, MANUAL

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223025032529%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3025032529