Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009896984

FEI Number

3009896984

Entity Name

Vivify Health Inc.

City/State/Country

Eden Prairie, MN, US

Establishment Address

1 Health Drive, MN103-0400, Eden Prairie, MN 55344, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

UHG (Owner Number: 10042285)

Owner / Operator Contact Address

1 Health Drive, Eden Prairie, MN 55344, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222398

PMA Number

N/A

All Registered Proprietary Names

Care Team Portal Vivify Care Team Portal

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRG	Transmitters And Receivers, Physiological Signal, Radiofrequency	Cardiovascular	Class 2	870.2910	2023-02-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UHG

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K131913	Philips Medizin Systeme Boeblingen GmbH	INTELLIVUE CL SPO2 POD AND CL NBP POD, PHILIPS INTELLIVUE PATIENT MONITORS MP5, MP5T, MP5SC	2013-11-26

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3012302888	QUIPMENT INC.	Kennesaw, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009896984. Last updated year: 2026. Please use registration number 3009896984 when referencing this establishment in official correspondence.