Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9613073

FEI Number

3003927064

Entity Name

SAHIROUN (PVT) LTD.

City/State/Country

SIALKOT Punjab, PK

Establishment Address

WAZIRABAD ROAD, RAHIMPUR, UGOKI, SIALKOT Punjab 51310, PK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SAHIROUN (PVT) LTD. (Owner Number: 9022104)

Owner / Operator Contact Address

WAZIRABAD ROAD, RAHIMPUR, UGOKI,, SIALKOT, PK-PB 51050, PK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DOYEN, BALFOUR, LANGENBECK GENERAL NEEDLE HOLDER ALL KINDS Operating Scissors CARTRIDGE SYRINGE ALL TYPES GENERAL NOVA, PRIMA, VISIO ENDOTRACHEAL FRAZIER, POOL, YANKAUER MASTERGLIDE, ECONOGLIDE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2006-06-07
HAO	Instrument, Surgical, Non-Powered	Neurology	Class 1	882.4535	2003-07-03
FHQ	Holder, Needle, Gastroenterologic	Gastroenterology, Urology	Class 1	876.4730	2006-06-07
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2006-06-07
EIC	Syringe, Periodontic, Endodontic, Irrigating	Dental	Class 1	872.4565	2006-06-07
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2006-06-07
KAI	Mirror, Ent	Ear, Nose, Throat	Class 1	874.4420	2006-06-07
BWB	Forceps, Tube Introduction	Anesthesiology	Class 1	868.5780	1995-08-29
JZF	Tube, Ear Suction	Ear, Nose, Throat	Class 1	874.4420	2006-06-07
BSR	Stylet, Tracheal Tube	Anesthesiology	Class 1	868.5790	1995-08-29

Official Correspondent

No official correspondent registered.

US Agent Details

ALANP.SCHWARTZ Business: MDI CONSULTANTS, INC. Email: ALAN@MDICONSULTANTS.COM Phone: (516) 482

Related Public Records

Same Entity

SAHIROUN (PVT) LTD.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K922626	Andronic Devices, Ltd.	ADEPT INSTRUMENT POSITIONING ACCESSORY	1992-10-19
K820290	The Anspach Effort, Inc.	SELF RETAINING RETRACTOR FOR HAND SURG	1982-03-05
K760422	Cutter Laboratories, Inc.	SURGICAL RETRACTOR	1976-08-23
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2014	Aesculap, Inc.	1	UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

Similar Registrations

Registration Number	Establishment Name	Location
3011050528	FREEHOLD SURGICAL, INC.	New Hope, PA, US
3021006167	KIMS MED CO., LTD.	Gwangju, KR
3045009502	WISDOM MEDICAL TECHNOLOGY (SHANGHAI) CO., LTD	Shanghai, CN
3032847175	BIOPHYX SURGICAL, INC.	Edgewater, MD, US
9681129	BEMA-GMBH & CO. KG	EMMINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9613073. Last updated year: 2026. Please use registration number 9613073 when referencing this establishment in official correspondence.