Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8022265

FEI Number

3002861325

Entity Name

GLOBALMED, INC.

City/State/Country

TRENTON Ontario, CA

Establishment Address

155 N. MURRAY ST., TRENTON Ontario K8V5R5, CA

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Molded Devices, Inc. (Owner Number: 10058611)

Owner / Operator Contact Address

740 W Knox Road, Tempe, AZ 85284, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Disposable Breathing Circuit Patient Assister Single Patient Breathing Tube Slimline Tubing Standard Tubing Clear Grey Single Patient Breathing Tube Filter Bacterial Breathing Circuit Tube, Smoke Removal, Endoscopic BALLARD* Flex Connector BALLARD* Flex Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CAI	Circuit, Breathing (W Connector, Adaptor, Y Piece)	Anesthesiology	Class 1	868.5240	2022-12-16
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2022-12-16
JAY	Support, Breathing Tube	Anesthesiology	Class 1	868.5280	2022-12-16
CAH	Filter, Bacterial, Breathing-Circuit	Anesthesiology	Class 2	868.5260	2022-12-16
FCZ	Tube, Smoke Removal, Endoscopic	Gastroenterology, Urology	Class 1	876.1500	2022-12-16
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2025-09-18

Official Correspondent

No official correspondent registered.

US Agent Details

Samuel Brayton Business: Molded Devices, Inc., dba Aptyx Email: sbrayton@aptyx.com Phone: (518) 6360303

Related Public Records

Same Entity

Molded Devices, Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1223009	MDI East, Inc., dba Medefab	JAFFREY, NH, US
3006686250	Guangzhou Schauenburg-Truplast Hose Technology Ltd.	Guangzhou Guangdong, CN
3015146495	MOLDED DEVICES, INC.	Tempe, AZ, US
1321175	BATES INDUSTRIES	S Glens Falls, NY, US
3011324393	MEDICAL MURRAY, INC.	Charlotte, NC, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K962045	Mallinckrodt Medical	ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT	1996-11-26

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0033-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube with Bird adapter, oxygen supply tubing, sideport connector with adjustable bleed valve, and 40 cm H2O Popoff elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83124-2
Z-0034-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, ported elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83100-24
Z-0035-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, 40 cm H2O Popoff elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83144-24
Z-0036-04	VIASYS Med Systems	1	Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120
Z-0037-04	VIASYS Med Systems	1	Sideport Kit, consisting of an adjustable sideport valve and an O2 port elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83166

Similar Registrations

Registration Number	Establishment Name	Location
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3030446844	PLATINUM FOCUS GROUP LTD.	London London, City of, GB
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8022265. Last updated year: 2026. Please use registration number 8022265 when referencing this establishment in official correspondence.