FDA Device Establishments · JSON-LD · Markdown
FEI 3016566173 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3016566173 |
|---|---|
| Owner / Operator | Kinvent Biomecanique SAS (#10062556) |
| Address | 6 Rue de Pommessargues, Montepellier Herault, 34000, FR |
| Mandatory US Agent | FDA Listing Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DRX |
| Regulation § (21 CFR) | 870.2360 |
| Proprietary names | K-myo x1000 patches pack; K Myo x1000 patches pack; K Myo Accessories |
Source: openFDA. Public-domain (CC0).