Data / Medical devices / Vietnam / Global Resources (vietnam) Group Limited Company

Global Resources (vietnam) Group Limited Company: FDA-registered device maker in Hai Phong City, Vietnam, 2 510(k) clearances

Name: Global Resources (vietnam) Group Limited Company FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Global Resources (vietnam) Group Limited Company is registered with the FDA (registration 3014925393) in Hai Phong City, Vietnam. It lists 27 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 18, 2025. Registered through 2027. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Global Resources (vietnam) Group Limited Company

FDA registration number: 3014925393
Address: Nhan Lap Village, Tan Minh Commune, Hai Phong City, Vietnam, 04000
Owner or operator: Global Resources (Vietnam) Group Limited Company (10058607)
Roles: Contract manufacturer, Contract sterilizer, Manufacturer
First device listed: October 14, 2018
Registered through: 2027
Brand names listed: Alleset, CHARLES ATKINS & CO, ComfortGuard, Drape, patient, ophthalmic, GRI-Alleset, Halyard, Invenio, Opt-Shield Air Supine and more

Devices it lists

Device	Product code	Class	Role	Source
Angiography/Angioplasty Kit	OEQ	2	Manufacturer	accessdata.fda.gov
Basin, Emesis	FNY	1	Contract manufacturer	accessdata.fda.gov
Battery-Powered Instruments Charged Through Sterile Barriers	SAM	1	Contract manufacturer	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Contract manufacturer	accessdata.fda.gov
Cardiovascular Procedure Kit	OEZ	2	Manufacturer	accessdata.fda.gov
Ct Biopsy Tray	OFG	2	Manufacturer	accessdata.fda.gov
D And C Tray	PKF	N	Manufacturer	accessdata.fda.gov
Drape, Patient, Ophthalmic	HMT	2	Contract manufacturer	accessdata.fda.gov
Drape, Surgical, Exempt	PUI	2	Contract manufacturer, Contract sterilizer	accessdata.fda.gov
Ear, Nose, And Throat Surgical Tray	OGR	1	Manufacturer	accessdata.fda.gov
Eye Tray	OJK	2	Manufacturer	accessdata.fda.gov
Fiber, Medical, Absorbent	FRL	1	Contract manufacturer	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Contract manufacturer	accessdata.fda.gov
General Surgery Tray	LRO	2	Manufacturer	accessdata.fda.gov
Gown, Isolation, Surgical	FYC	2	Contract manufacturer	accessdata.fda.gov
Gown, Surgical	FYA	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Gynecological Laparoscopic Kit	OHD	2	Manufacturer	accessdata.fda.gov
Labor And Delivery Kit	MLS	2	Manufacturer	accessdata.fda.gov
Laparoscopy Kit	FDE	2	Contract manufacturer	accessdata.fda.gov
Mask, Surgical	FXX	2	Manufacturer	accessdata.fda.gov
Neurological Tray	OJG	1	Contract manufacturer	accessdata.fda.gov
Non-Surgical Gown	OEA	1	Contract manufacturer	accessdata.fda.gov
Restraint, Protective	FMQ	1	Contract manufacturer	accessdata.fda.gov
Support, Patient Position	CCX	1	Contract manufacturer	accessdata.fda.gov
System, X-Ray, Fluoroscopic, Image-Intensified	JAA	2	Contract manufacturer	accessdata.fda.gov
Transtibial Anterior Cruciate Ligament Kit	PPQ	2	Manufacturer	accessdata.fda.gov
Urinary Irrigation Kit	PPF	2	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 18, 2025	K250082	Procedure mask/Surgical mask/Face mask	FXX	Substantially Equivalent	Winner Medical Co., Ltd.	accessdata.fda.gov
December 8, 2017	K172445	RoyalGuard Surgical Gown, i600, Breathable	FYA	Substantially Equivalent	Gri Medical & Electrical Technology Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated June 18, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.