Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009595635

FEI Number

3009595635

Entity Name

GlobeStar Systems, Inc

City/State/Country

Toronto Ontario, CA

Establishment Address

7 Kodiak Crescent, Suite 100, Toronto Ontario M3J 3E5, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Connexall USA, Inc. (Owner Number: 10035909)

Owner / Operator Contact Address

4571 Broadway Street, Boulder, CO 80304, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K112650

PMA Number

N/A

All Registered Proprietary Names

Connexall Suite of Software Products CNSPRO-U CNS-LITE CNS-CARE-U

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MSX	System, Network And Communication, Physiological Monitors	Cardiovascular	Class 2	870.2300	2012-05-10

Official Correspondent

Mary DiGioia

US Agent Details

Mary DiGioia Business: Connexall USA Email: mdigioia@connexall.com Phone: (866) 5563377

Related Public Records

Same Entity

Connexall USA, Inc.

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
K973527	Data Critical Corp.	CARDIO-PAGER SYSTEM	1998-03-31
K182637	Philips Medizin Systeme Boeblingen GmbH	Philips IntelliVue XDS Software	2019-04-26

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2080783	NIHON KOHDEN AMERICA, INC.	Irvine, CA, US
3013500228	Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.	Tsimshatsui, Kowloon, HK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009595635. Last updated year: 2026. Please use registration number 3009595635 when referencing this establishment in official correspondence.