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Goldstar Medical Instruments: FDA-registered device maker in SIALKOT Punjab, Pakistan, 2 510(k) clearances

Name: Goldstar Medical Instruments FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Goldstar Medical Instruments is registered with the FDA (registration 3000126234) in SIALKOT Punjab, Pakistan. It lists 20 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 6, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3000126234
Address: Hayat Centre, Khadim Ali Road Box 2098, SIALKOT Punjab, Pakistan, 51310
Owner or operator: Goldstar Medical Instruments (9053992)
Roles: Contract manufacturer, Exporter to the US, Manufacturer
First device listed: November 25, 2002
Registered through: 2026
Brand names listed: Adson Forcep (disposable), Astra-Vue, Astra-Vue ALTIS, Astra-Vue LITE, Astra-Vue PRO, Astra-Vue ULTRA, Blotting Towel, Disposable CSR Wrap and more

Devices it lists

Device	Product code	Class	Role	Source
Bedding, Disposable, Medical	KME	1	Exporter to the US	accessdata.fda.gov
Device, Fixation, Tracheal Tube	CBH	1	Manufacturer	accessdata.fda.gov
Forceps	HTD	1	Manufacturer	accessdata.fda.gov
Forceps, General & Plastic Surgery	GEN	1	Manufacturer	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Exporter to the US	accessdata.fda.gov
Gown, Examination	FME	1	Exporter to the US	accessdata.fda.gov
Holder, Needle; Orthopedic	HXK	1	Manufacturer	accessdata.fda.gov
Hook, Tracheal	KCH	1	Manufacturer	accessdata.fda.gov
Laceration Tray	PKD	1	Manufacturer	accessdata.fda.gov
Laryngoscope, Rigid	CCW	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Needle, Hypodermic, Single Lumen	FMI	2	Exporter to the US	accessdata.fda.gov
Ring Cutter	FNS	1	Manufacturer	accessdata.fda.gov
Scissors, Ophthalmic	HNF	1	Manufacturer	accessdata.fda.gov
Scissors, Orthopedic, Surgical	HRR	1	Manufacturer	accessdata.fda.gov
Speculum, Vaginal, Metal	HDF	1	Manufacturer	accessdata.fda.gov
Stylet, Tracheal Tube	BSR	1	Manufacturer	accessdata.fda.gov
Syringe, Antistick	MEG	2	Exporter to the US	accessdata.fda.gov
Syringe, Cartridge	EJI	2	Manufacturer	accessdata.fda.gov
Syringe, Periodontic, Endodontic, Irrigating	EIC	1	Manufacturer	accessdata.fda.gov
Syringe, Piston	FMF	2	Exporter to the US	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
September 6, 2019	K183665	Safety Needles, Sterile Syringe, Sterile Syringe with Safety Needle, Sterile Syringe with Needle, Hypodermic Needle for Single Use	MEG	Substantially Equivalent	Jiangsu Micsafe Medical Technology Co., Ltd.	accessdata.fda.gov
November 6, 2012	K120659	HU-FRIEDY DENTAL CARTRIDGE SYRINGE	EJI	Substantially Equivalent	Hu-Friedy Mfg. Co., LLC	accessdata.fda.gov

Compare with other makers

Updated September 6, 2019. 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.