FDA Device Establishments · JSON-LD · Markdown
FEI 2518410 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 2518410 |
|---|---|
| Owner / Operator | GULDEN OPHTHALMICS INC (#2518410) |
| Address | 225 CADWALADER AVE., Elkins Park, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HLP |
| Regulation § (21 CFR) | 886.1880 |
| Proprietary names | Fly Stereo Acuity Test; Fixi-Tic; Butterfly Stereo Acuity Test |
Source: openFDA. Public-domain (CC0).