FDA Device Establishments · JSON-LD · Markdown
FEI 3031182687 · Manufacture Medical Device · Status: Active
| FEI Number | 3031182687 |
|---|---|
| Owner / Operator | Wuhan Qolight Technology Co., Ltd. (#10090355) |
| Address | Room 301, Building No. 2, East Lake High-tech Industry Innovation Base, 9 Miaoshan Avenue, Jiangxia, Wuhan Hubei, 430299, CN |
| Mandatory US Agent | UGK-LVM UNITED INC |
| Registration expiry | 2027 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GFE |
| Regulation § (21 CFR) | 878.4820 |
| Proprietary names | InjeX; InjeX Lite; InjeX Pro |
Source: openFDA. Public-domain (CC0).