FDA Device Establishments · JSON-LD · Markdown
FEI 3010910479 · Manufacture Medical Device · Status: Active
| FEI Number | 3010910479 |
|---|---|
| Owner / Operator | Essilor of America, Inc (#8010073) |
| Address | AV. ETO141009IN6, AV. WASHINGTON NO. 3701, EDIFICIO 19, MOSAICO NORTE, CHIHUAHUA,, CHIHUAHUA, 31103, MX |
| Mandatory US Agent | EssilorLuxottica |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQG |
| Regulation § (21 CFR) | 886.5844 |
| Proprietary names | TruClear; Avance; DEFINITY 2; Xperio; Essilor Ideal; Varilux; Small Fit; Trivex; VARILUX-2; Presio i Approval |
Source: openFDA. Public-domain (CC0).