FDA Device Establishments · JSON-LD · Markdown
FEI 3009432160 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3009432160 |
|---|---|
| Owner / Operator | anaxdent North America (#10039879) |
| Address | 406 I ST NW ARDMORE, Ardmore, OK, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | EIH |
| Regulation § (21 CFR) | 872.6660 |
| Proprietary names | Soprano Surface; Soprano |
Source: openFDA. Public-domain (CC0).