FDA Device Establishments · JSON-LD · Markdown
FEI 3045320731 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3045320731 |
|---|---|
| Owner / Operator | Aurora GP Lab Inc (#10095822) |
| Address | 13765 W Auto Dr Ste 124, Goodyear, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MUW |
| Regulation § (21 CFR) | 886.5916 |
| Proprietary names | See Z Tangent (roflufocon D) Rigid Gas Permeable Contact Lens for Orthokeratology - Daily Wear; OrthCyl (roflufocon D) Rigid Gas Permeable Contact Lens for Orthokeratology - Daily Wear; See Z (roflufocon D) Rigid Gas Permeable Contact Lens for Orthokeratology - Daily Wear; OrthCyl X-Toric (roflufocon D) Rigid Gas Permeable Contact Lens for Orthokeratology - Daily Wear |
Source: openFDA. Public-domain (CC0).