FDA Device Establishments · JSON-LD · Markdown
FEI 3022019579 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3022019579 |
|---|---|
| Owner / Operator | Amparo Prosthetics, Inc. (#10084709) |
| Address | 2111 West Alexander St, West Valley City, UT, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | ISP |
| Regulation § (21 CFR) | 890.3420 |
| Proprietary names | Resilience Button Valve Kit; One-way Valve |
Source: openFDA. Public-domain (CC0).