FDA Device Establishments · JSON-LD · Markdown
FEI 3025591939 · Manufacture Medical Device Remanufacture Medical Device · Status: Active
| FEI Number | 3025591939 |
|---|---|
| Owner / Operator | KINVENT Hellas (#10086801) |
| Address | 14km Thessaloniki, Neon Moudanion, plot 1490, Thermi Kentriki Makedonia, 57001, GR |
| Mandatory US Agent | FDA Listing Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQX |
| Regulation § (21 CFR) | 888.1500 |
| Proprietary names | KFORCE Grip (LBB), KFORCE Muscle Controller (LBB), KFORCE Link (LBB), KFORCE Sens (KQX), KFORCE Bubble (LBB), KFORCE Pla; K-Grip (KFORCE Grip), K-Push (KFORCE Muscle Controller), K-Pull (KFORCE Link), K-Move (KFORCE Sens), K-Bubble (KFORCE Bu |
Source: openFDA. Public-domain (CC0).