FDA Device Establishments · JSON-LD · Markdown
FEI 3009225484 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3009225484 |
|---|---|
| Owner / Operator | Zyllion, Inc. (#10045182) |
| Address | 26439 Rancho Pkwy S, Unit 175, Lake Forest, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | ISA |
| Regulation § (21 CFR) | 890.5660 |
Source: openFDA. Public-domain (CC0).