FDA Device Establishments · JSON-LD · Markdown
FEI 3010521015 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3010521015 |
|---|---|
| Owner / Operator | Fistula Solution Corporation (#10045153) |
| Address | 10604 230TH ST N, Scandia, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EZS |
| Regulation § (21 CFR) | 876.5900 |
| Proprietary names | Wound Crown; Isolator Strip; Fistula Funnel |
Source: openFDA. Public-domain (CC0).