Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010876604

FEI Number

3010876604

Entity Name

GARRETT HEILBRUN TECHNOLOGY PARTNERS, LLC DBA COBALT PRODUCT SOLUTIONS

City/State/Country

Plano, TX, US

Establishment Address

1825 E Plano Pkwy, Suite 200, Plano, TX 75074, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Garrett Heilbrun Technology Partners, LLC dba Cobalt Product (Owner Number: 10059983)

Owner / Operator Contact Address

1825 E Plano Pkwy, Suite 200, Plano, TX 75074, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Deepview Snapshot Imaging System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LGZ	Warmer, Thermal, Infusion Fluid	General Hospital	Class 2	880.5725	2019-03-17
BSB	Warmer, Blood, Non-Electromagnetic Radiation	Hematology	Class 2	864.9205	2019-03-17
FXN	Tape, Camera, Surgical	General, Plastic Surgery	Class 1	878.4160	2024-01-18

Official Correspondent

Robert Heilbrun

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Garrett Heilbrun Technology Partners, LLC dba Cobalt Product

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
K090508	Belmont Instrument Corp.	THE BELMONT BUDDY LITE FLUID WARMER	2009-03-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010876604. Last updated year: 2026. Please use registration number 3010876604 when referencing this establishment in official correspondence.