FDA Device Establishments · JSON-LD · Markdown
FEI 3027686079 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3027686079 |
|---|---|
| Owner / Operator | The Initiative LLC., DBA KyphoLift (#10088492) |
| Address | 10352 S River Heights Dr, Suite 104, South Jordan, UT, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KXH |
| Regulation § (21 CFR) | 892.1830 |
| Proprietary names | KyphoLift |
Source: openFDA. Public-domain (CC0).