FDA Device Establishments · JSON-LD · Markdown
FEI 3004145084 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3004145084 |
|---|---|
| Owner / Operator | OPTIK K & R Inc. (#10045451) |
| Address | 425 Midwest Road, Toronto Ontario, M1P3A6, CA |
| Mandatory US Agent | The Vision Council |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQZ |
| Regulation § (21 CFR) | 886.5842 |
| Proprietary names | Ophthalmic Spectacle Frame |
Source: openFDA. Public-domain (CC0).