FDA Device Establishments · JSON-LD · Markdown
FEI 3031081959 · Manufacture Medical Device · Status: Active
| FEI Number | 3031081959 |
|---|---|
| Owner / Operator | RetinaLogik Inc. (#10090291) |
| Address | 3655 36 street NW, Calgary Alberta, T2L 1Y8, CA |
| Mandatory US Agent | QA/RA CONSULTING GROUP, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HIT |
| Regulation § (21 CFR) | 886.1170 |
| Proprietary names | RVF200 |
Source: openFDA. Public-domain (CC0).