# VIEWORKS CO., LTD.

FEI: 3006013411
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Vieworks Co., Ltd. (#10024523)

Address: 41-3, Burim-ro 170beon-gil, Dongan-gu, Anyang-si Gyeonggi, 14055, KR

Mandatory US Agent: Vieworks America Ltd.

## Products

Total registered: 1
Top product codes: MQB
Regulation §: 892.1680

Proprietary names: VWD-1717A, VIVIX-S F series, VIVIX-S FW (Model: FXRD-4343FAW, FXRD-3643FAW, FXRD-2530FAW), VWD-1417A, Saturn 8000, F3025-AW

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006013411%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006013411