FDA Device Establishments · JSON-LD · Markdown
FEI 3009538853 · Manufacture Medical Device · Status: Active
| FEI Number | 3009538853 |
|---|---|
| Owner / Operator | Kinova (#10045047) |
| Address | 4333 Grande-Allee, Boisbriand Quebec, J7H 1M7, CA |
| Mandatory US Agent | Partners in Medicine LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KNO |
| Regulation § (21 CFR) | 890.3910 |
| Proprietary names | Kinova Lift Arm |
Source: openFDA. Public-domain (CC0).