FDA Device Establishments · JSON-LD · Markdown
FEI 3007284313 · Manufacture Medical Device · Status: Active
| FEI Number | 3007284313 |
|---|---|
| Owner / Operator | W. L. GORE & ASSOCIATES, INC. (#9925013) |
| Address | 32360 N. North Valley Parkway, Phoenix, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DXZ |
| Regulation § (21 CFR) | 870.3470 |
| Proprietary names | GORE PRECLUDE pericardial membrane |
Source: openFDA. Public-domain (CC0).