FDA Device Establishments · JSON-LD · Markdown
FEI 3010675856 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3010675856 |
|---|---|
| Owner / Operator | Kinetec USA, Inc. (#10045573) |
| Address | N174W21475 Alcan Drive, Jackson, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | ILO |
| Regulation § (21 CFR) | 890.5720 |
Source: openFDA. Public-domain (CC0).