FDA Device Establishments · JSON-LD · Markdown
FEI 1000188353 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1000188353 |
|---|---|
| Owner / Operator | MENICON CO. LTD. (#9001029) |
| Address | 21-19 AOI, 3-CHOME, NAKA-KU, NAGOYA Aichi, 460-0006, JP |
| Mandatory US Agent | MENICON AMERICA, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQD |
| Regulation § (21 CFR) | 886.5916 |
Source: openFDA. Public-domain (CC0).