FDA Device Establishments · JSON-LD · Markdown
FEI 3032577207 · Complaint File Establishment per 21 CFR 820.198 Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3032577207 |
|---|---|
| Owner / Operator | Positrigo AG (#10091382) |
| Address | Technoparkstrasse 1, Zurich, 8005, CH |
| Mandatory US Agent | Positrigo Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KPS |
| Regulation § (21 CFR) | 892.1200 |
| Proprietary names | NeuroLF Seat; NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced) |
Source: openFDA. Public-domain (CC0).