Data / Medical devices / Pakistan / Track Of Surgical

Track Of Surgical: FDA-registered device maker in SIALKOT Punjab, Pakistan, 1 510(k) clearance

Name: Track Of Surgical FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Track Of Surgical is registered with the FDA (registration 9614068) in SIALKOT Punjab, Pakistan. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 17, 1998. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 9614068
FEI number: 3008350177
Address: Commissioner RD., SIALKOT Punjab, Pakistan, 51310
Owner or operator: TRACK OF SURGICAL (9030794)
Roles: Manufacturer
First device listed: June 17, 1997
Registered through: 2026
Brand names listed: Medgyn Products INC, Medgyn Products Inc

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Implant, Dental, Endosseous	NDP	1	Manufacturer	accessdata.fda.gov
Cane	IPS	1	Manufacturer	accessdata.fda.gov
Cup, Prophylaxis	EHK	1	Manufacturer	accessdata.fda.gov
Curette, Uterine	HCY	1	Manufacturer	accessdata.fda.gov
Dilator, Cervical, Fixed Size	HDQ	1	Manufacturer	accessdata.fda.gov
Forceps	HTD	1	Manufacturer	accessdata.fda.gov
Forceps, Biopsy, Gynecological	HFB	1	Manufacturer	accessdata.fda.gov
Forceps, Tooth Extractor, Surgical	EMG	1	Manufacturer	accessdata.fda.gov
Instrument, Manual, Surgical, General Use	MDM	1	Manufacturer	accessdata.fda.gov
Punch, Biopsy, Surgical	EME	1	Manufacturer	accessdata.fda.gov
Retractor, All Types	EIG	1	Manufacturer	accessdata.fda.gov
Retractor, Vaginal	HDL	1	Manufacturer	accessdata.fda.gov
Scissors, General, Surgical	LRW	1	Manufacturer	accessdata.fda.gov
Scissors, Surgical Tissue, Dental	EGN	1	Manufacturer	accessdata.fda.gov
Sound, Uterine	HHM	1	Manufacturer	accessdata.fda.gov
Speculum, Non-Illuminated	FXE	1	Manufacturer	accessdata.fda.gov
Speculum, Vaginal, Metal	HDF	1	Manufacturer	accessdata.fda.gov
Tenaculum, Uterine	HDC	2	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
March 17, 1998	K980247	GYNEX IRIS HOOK, GYNEX ANGLE HOOK, GYNEX EMMETT TENACULUM	HDC	Substantially Equivalent	Gynex Corp.	accessdata.fda.gov

Compare with other makers

Updated March 17, 1998. 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.