FDA Device Establishments · JSON-LD · Markdown
FEI 3013398957 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3013398957 |
|---|---|
| Owner / Operator | COOPERVISION, INC. (#9929062) |
| Address | 2120 W. Guadalupe Rd., Gilbert, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 3 |
| Product codes (top 20) | HQD, NUU, MWL |
| Regulation § (21 CFR) | 886.5916 |
| Proprietary names | Paragon RG-4; Paragon CRT100; Paragon CRT; Paragon CRT Dual Axis; FluoroPerm60; HDS; HDS100; FluoroPerm151; FluoroPerm92; FluoroPerm30 |
Source: openFDA. Public-domain (CC0).