FDA Device Establishments · JSON-LD · Markdown
FEI 3013552417 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3013552417 |
|---|---|
| Owner / Operator | Kico Knee Innovation Company (#10054916) |
| Address | Unit 1, 25 Frenchs Forest Rd E, Frenchs Forest New South Wales, 2086, AU |
| Mandatory US Agent | Encore Medical, L.P. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HXB |
| Regulation § (21 CFR) | 888.4540 |
| Proprietary names | KICo Probe |
Source: openFDA. Public-domain (CC0).