FDA Device Establishments · JSON-LD · Markdown
FEI 3006013411 · 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 · Status: Active
| FEI Number | 3006013411 |
|---|---|
| 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. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQB |
| Regulation § (21 CFR) | 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. Public-domain (CC0).