FDA Device Establishments · JSON-LD · Markdown
FEI 3003895329 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active
| FEI Number | 3003895329 |
|---|---|
| Owner / Operator | SURESTEP, LLC (#10028081) |
| Address | 17530 DUGDALE DR, South Bend, IN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | MVA, OAN |
| Regulation § (21 CFR) | 882.5970 |
Source: openFDA. Public-domain (CC0).