FDA Device Establishments · JSON-LD · Markdown
FEI 3014758755 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3014758755 |
|---|---|
| Owner / Operator | KANEKA AMERICAS HOLDING INC (#10095053) |
| Address | 7979 Gateway Blvd, Newark, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | KRA, QJP |
| Regulation § (21 CFR) | 870.1210, 870.1250 |
| Proprietary names | Surfrider 13 Microcatheter |
Source: openFDA. Public-domain (CC0).