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Medical Devices (pvt) Ltd.: FDA-registered device maker in Sialkot Punjab, Pakistan, 1 510(k) clearance

Name: Medical Devices (pvt) Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Medical Devices (pvt) Ltd. is registered with the FDA (registration 9614084) in Sialkot Punjab, Pakistan. It lists 21 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 19, 2010. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 9614084
FEI number: 3001620388
Address: Wazirabad Road, Ugoki., Sialkot Punjab, Pakistan, 51050
Owner or operator: MEDICAL DEVICES (PVT) LTD. (9031998)
Roles: Manufacturer
First device listed: October 27, 1997
Registered through: 2026
Brand names listed: -UROLOGY, CARTRIDGE DENTAL SYRINGE, CHEST PIECES, Connectors and Prisms, DERMASCOPE, FLOWMETER AND ADAPTOR, FORCEPS GENERAL AND PLASTIC SURGERY, FRAZIER and more

Devices it lists

Device	Product code	Class	Role	Source
Connector, Airway (Extension)	BZA	1	Manufacturer	accessdata.fda.gov
Flowmeter, Tube, Thorpe, Back-Pressure Compensated	CAX	1	Manufacturer	accessdata.fda.gov
Forceps	HTD	1	Manufacturer	accessdata.fda.gov
Hemostat	HRQ	1	Manufacturer	accessdata.fda.gov
Holder, Needle, Gastroenterologic	FHQ	1	Manufacturer	accessdata.fda.gov
Instrument, Surgical, Non-Powered	HAO	1	Manufacturer	accessdata.fda.gov
Laryngoscope, Rigid	CCW	1	Manufacturer	accessdata.fda.gov
Light, Microscope	IBJ	1	Manufacturer	accessdata.fda.gov
Mirror, Ent	KAI	1	Manufacturer	accessdata.fda.gov
Ophthalmoscope, Battery-Powered	HLJ	2	Manufacturer	accessdata.fda.gov
Otoscope	ERA	1	Manufacturer	accessdata.fda.gov
Regulator, Pressure, Gas Cylinder	CAN	1	Manufacturer	accessdata.fda.gov
Retractor	GAD	1	Manufacturer	accessdata.fda.gov
Scissors, General, Surgical	LRW	1	Manufacturer	accessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	HOY	1	Manufacturer	accessdata.fda.gov
Speculum, Vaginal, Metal	HDF	1	Manufacturer	accessdata.fda.gov
Stethoscope Head	BZS	1	Manufacturer	accessdata.fda.gov
Stylet, Tracheal Tube	BSR	1	Manufacturer	accessdata.fda.gov
Support, Breathing Tube	JAY	1	Manufacturer	accessdata.fda.gov
Syringe, Periodontic, Endodontic, Irrigating	EIC	1	Manufacturer	accessdata.fda.gov
Tube, Ear Suction	JZF	1	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
November 19, 2010	K093495	OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS	HLJ	Substantially Equivalent	American Diagnostic Corp.	accessdata.fda.gov

Compare with other makers

Updated November 19, 2010. 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.