Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027686079

FEI Number

3027686079

Entity Name

THE INITIATIVE LLC., DBA KyphoLift

City/State/Country

South Jordan, UT, US

Establishment Address

10352 S River Heights Dr, Suite 104, South Jordan, UT 84095, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

The Initiative LLC., DBA KyphoLift (Owner Number: 10088492)

Owner / Operator Contact Address

10352 S River Heights Dr, Suite 104, South Jordan, UT 84095, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KyphoLift

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXH	Cradle, Patient, Radiologic	Radiology	Class 1	892.1830	2023-08-01

Official Correspondent

Andrew Hartman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Initiative LLC., DBA KyphoLift

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027686079. Last updated year: 2026. Please use registration number 3027686079 when referencing this establishment in official correspondence.