FDA Device Establishments · JSON-LD · Markdown
FEI 3014498660 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3014498660 |
|---|---|
| Owner / Operator | Nexalin Technology, Inc. (#10057669) |
| Address | 1776 Yorktown, Ste 550, Houston, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QJQ |
| Regulation § (21 CFR) | 882.5800 |
| Proprietary names | Nexalin ADI; Patient Cable; Electrode Set |
Source: openFDA. Public-domain (CC0).