Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023191945

FEI Number

3023191945

Entity Name

FRESH VALLEY

City/State/Country

Gujrat Punjab, PK

Establishment Address

Zaib Plaza, Rehman Shaheed Road, Near Bank Alfalah, Gujrat Punjab 50700, PK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Fresh Valley (Owner Number: 10089748)

Owner / Operator Contact Address

Zaib Plaza, Rehman Shaheed Road, Near Bank Alfalah, Gujrat, PK-PB 50700, PK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cannula Trocar Swipe Drape KIT Retractor CSR WRAP SPECULUM Nab

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2024-01-04
DRC	Trocar	Cardiovascular	Class 2	870.1390	2024-01-04
HYA	Forceps, Wire Holding	General, Plastic Surgery	Class 1	878.4800	2025-07-31
LDZ	Fixative, Alcohol Containing	Pathology	Class 1	864.4010	2026-01-15
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2026-01-15
PUI	Drape, Surgical, Exempt	General, Plastic Surgery	Class 2	878.4370	2026-01-15
GEN	Forceps, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2024-01-04
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2025-07-31
FPY	Sheet, Burn	General Hospital	Class 1	880.5180	2026-04-14
NAD	Dressing, Wound, Occlusive	General, Plastic Surgery	Class 1	878.4020	2026-01-15
HDF	Speculum, Vaginal, Metal	Obstetrics/Gynecology	Class 1	884.4520	2025-03-14
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2024-01-04

Official Correspondent

Junaid Rasool

US Agent Details

Imran Tarar Email: Itarar16@gmail.com Phone: (773) 8177965

Related Public Records

Same Entity

Fresh Valley

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
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09
K761138	Zeus Scientific, Inc.	FA TISSUE FIXATIVE & WASH SET	1978-01-06
K842913	E K Ind., Inc.	WRIGHT STAIN FIXATIVE	1984-09-07
K851170	The Huxley Instrument Corp.	DISSECTING TWEEZER #283-72PCS. SS 410	1985-04-25
K821248	Conphar, Inc.	ROCHESTER PEAN FORCEPS	1982-05-28

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.
Z-0013-2019	COVIDIEN LLC	1	Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019	COVIDIEN LLC	1	Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019	COVIDIEN LLC	1	Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019	COVIDIEN LLC	1	Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

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1526439	DEPUY SPINE, INC.	RAYNHAM, MA, US
1058584	Sterigenics US LLC	Charlotte, NC, US
1221763	ARCH Medical Solutions - Seabrook	SEABROOK, NH, US
8043496	REDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023191945. Last updated year: 2026. Please use registration number 3023191945 when referencing this establishment in official correspondence.