CHAPLET INTERNATIONAL

FDA Device Registration & Listing · Lahore Punjab, PK · Registration 3003998824

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3003998824
FEI Number
3003998824
Entity Name
CHAPLET INTERNATIONAL
City/State/Country
Lahore Punjab, PK
Establishment Address
Parwain Thay, Julke 28-Km Ferozepur Road, Lahore Punjab 53100, PK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Chaplet International (Pvt) Ltd (Owner Number: 10051298)
Owner / Operator Contact Address
Parwain Thay, Julke, 28-Km Ferozepur Road, Lahore, PK-PB 53100, PK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SCISSORS, ORTHOPEDIC, SURGICAL EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE HOLDER, NEEDLE, GASTROENTEROLOGIC PLATE, BASE, SHELLAC TRAY, SURGICAL, INSTRUMENT FORCEPS, WIRE HOLDING

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRR Scissors, Orthopedic, Surgical Orthopedic Class 1 888.4540 2016-03-01
KCX Epilator, High Frequency, Tweezer-Type General, Plastic Surgery Class 1 878.5360 2016-03-01
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 2016-03-01
EEA Plate, Base, Shellac Dental Class 1 872.6200 2016-03-01
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2016-03-01
HYA Forceps, Wire Holding General, Plastic Surgery Class 1 878.4800 2016-03-01

Official Correspondent

Anees Bhatti

US Agent Details

Muhammad Rashid Email: raza.rashid@onshoreadvisors.com Phone: (317) 8536072

Related Public Records

Same Entity

Chaplet International (Pvt) Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003998824. Last updated year: 2026. Please use registration number 3003998824 when referencing this establishment in official correspondence.
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