FDA Device Establishments · JSON-LD · Markdown
FEI 3049422862 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3049422862 |
|---|---|
| Owner / Operator | Pulmera Inc. (#10096327) |
| Address | 7th floor, 905 Pearl Parkway, Charlotte, NC, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | JAK, OWB |
| Regulation § (21 CFR) | 892.1750, 892.1650 |
| Proprietary names | C-beam system |
Source: openFDA. Public-domain (CC0).