FDA Device Establishments · JSON-LD · Markdown
FEI 3005172759 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3005172759 |
|---|---|
| Owner / Operator | ACCLARENT, INC. (#9068915) |
| Address | 7585 Irvine Center Dr, Irvine, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | LRC |
| Regulation § (21 CFR) | 874.4420 |
| Proprietary names | Relieva Spin Balloon Sinuplasty System |
Source: openFDA. Public-domain (CC0).