FDA Device Establishments · JSON-LD · Markdown
FEI 3021337298 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3021337298 |
|---|---|
| Owner / Operator | MIMOSA Diagnostics Inc. (#10083796) |
| Address | Unit 434, 366 Adelaide St East, Toronto Ontario, M5A3X9, CA |
| Mandatory US Agent | MIMOSA Diagnostics Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MUD |
| Regulation § (21 CFR) | 870.2700 |
| Proprietary names | MIMOSA Pro (previously Imager) |
Source: openFDA. Public-domain (CC0).