Establishment registration
THE INITIATIVE LLC., DBA KyphoLift
FDA establishment registration 3027686079 · South Jordan, US
Key facts
| Registration number | 3027686079 |
|---|---|
| Establishment name | THE INITIATIVE LLC., DBA KyphoLift |
| Owner/operator | The Initiative LLC., DBA KyphoLift |
| Owner/operator number | 10088492 |
| FEI number | 3027686079 |
| Address | 10352 S River Heights Dr |
| City | South Jordan |
| State | UT |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | KXH |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database