FDA Device Establishments · JSON-LD · Markdown
FEI 3009685869 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3009685869 |
|---|---|
| Owner / Operator | Reilly Foam Corporation (#10055051) |
| Address | 920 Frontenac RD, Naperville, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KXF |
| Regulation § (21 CFR) | 880.6025 |
| Proprietary names | Steris |
Source: openFDA. Public-domain (CC0).