FDA Device Establishments · JSON-LD · Markdown
FEI 3042953152 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3042953152 |
|---|---|
| Owner / Operator | Boulder iQ (#10094690) |
| Address | 5421 Western Ave, Boulder, CO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KRD |
| Regulation § (21 CFR) | 870.3300 |
| Proprietary names | Nitinol Enhanced Device (NED) |
Source: openFDA. Public-domain (CC0).