FDA Device Establishments · JSON-LD · Markdown
FEI 3023789889 · 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 | 3023789889 |
|---|---|
| Owner / Operator | Xerosguard Inc. (#10091548) |
| Address | 30th Floor, 360 Main Street, C/O MLT Aikins LLP, Winnipeg Manitoba, R3N 0P5, CA |
| Mandatory US Agent | Registrar Corp. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EIG |
| Regulation § (21 CFR) | 872.4565 |
| Proprietary names | Xerosguard |
Source: openFDA. Public-domain (CC0).