FDA Device Establishments · JSON-LD · Markdown
FEI 3004786509 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3004786509 |
|---|---|
| Owner / Operator | InterX Technologies (#10051305) |
| Address | 3465 Technology Dr., Suite A, Plano, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GXY |
| Regulation § (21 CFR) | 882.1320 |
| Proprietary names | InterX Self-Adhesive Dual Electrode - Non-Sterile |
Source: openFDA. Public-domain (CC0).