Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004936110

FEI Number

3004936110

Entity Name

Abbott Medical

City/State/Country

Atlanta, GA, US

Establishment Address

387 Nerem St Nw Ste 500, Atlanta, GA 30313, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ABBOTT LABORATORIES (Owner Number: 1415939)

Owner / Operator Contact Address

100 ABBOTT PARK RD., D-03Q3, AP52-1, Abbott Park, IL 60064, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P100045

All Registered Proprietary Names

CardioMEMS HF System CardioMEMS Hospital Electronics System CardioMEMS Patient Electronics System Merlin.net Patient Care Network Heart Failure Portal CardioMEMS PA Sensor and Delivery System CardioMEMS Hospital System CardioMEMS HERO Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MOM	System, Hemodynamic, Implantable	Unknown	Class 3	N/A	2018-02-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ABBOTT LABORATORIES

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004032053	Abbott S.r.l.	Milan Lombardy, IT
3011706799	Abbott Medical	Atlanta, GA, US
1628664	ABBOTT LABORATORIES	IRVING, TX, US
3023268435	Abbott Automation Solutions GmbH	Hamburg, DE
3001883144	St. Jude Medical Brasil Ltda.	Belo Horizonte Minas Gerais, BR

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0458-2026	Abbott Medical	3	Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400
Z-0459-2026	Abbott Medical	3	Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400
Z-0491-2025	Abbott Medical	3	Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, Sterile
Z-0492-2025	Abbott Medical	3	Abbott Navitor Transcatheter Aortic Heart Valve, 29 mm, NVTR-29, Sterile
Z-0493-2025	Abbott Medical	3	Abbot Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 29 mm, NVRO-29, Sterile

Similar Registrations

Registration Number	Establishment Name	Location
3005308195	SALINE LECTRONICS	Saline, MI, US
3011706799	Abbott Medical	Atlanta, GA, US
2916596	THORATEC CORP.	PLEASANTON, CA, US
3024985933	ENDOTRONIX (Naperville)	Naperville, IL, US
3038966819	UIM PRESSURE IMPLANT INC	Ypsilanti, MI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004936110. Last updated year: 2026. Please use registration number 3004936110 when referencing this establishment in official correspondence.