FDA Device Establishments · JSON-LD · Markdown
FEI 3016252795 · Manufacture Medical Device · Status: Active
| FEI Number | 3016252795 |
|---|---|
| Owner / Operator | Wondfo USA Co., Ltd. (#10028951) |
| Address | 6720 Cobra Way, San Diego, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | QMN |
| Proprietary names | WELLlife COVID-19 / Influenza A&B Test; WELLlife COVID-19 / Influenza A&B Home Test |
Source: openFDA. Public-domain (CC0).