FDA Device Establishments · JSON-LD · Markdown
FEI 3009843463 · Remanufacture Medical Device Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3009843463 |
|---|---|
| Owner / Operator | INOGEN, INC. (#9064201) |
| Address | 600 Shiloh Rd., Plano, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | SDT |
| Regulation § (21 CFR) | 868.5665 |
| Proprietary names | SIMEOX 200 Airway Clearance Device |
Source: openFDA. Public-domain (CC0).