FDA Device Establishments · JSON-LD · Markdown
FEI 3024682301 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Reprocess Single-Use Device · Status: Active
| FEI Number | 3024682301 |
|---|---|
| Owner / Operator | SureAx Medical, Corporation (#10086251) |
| Address | 11107 Roselle St 237, San Diego, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DQX |
| Regulation § (21 CFR) | 870.1330 |
| Proprietary names | SureAx Guide |
Source: openFDA. Public-domain (CC0).