Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027187888

FEI Number

3027187888

Entity Name

DOCTOR DEVICES

City/State/Country

Sialkot Punjab, PK

Establishment Address

Daska Road Boghra, Barkat Street, Sialkot, Sialkot Punjab 51310, PK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Doctor Devices (Owner Number: 10095377)

Owner / Operator Contact Address

Daska Road Boghra, Barkat Street, Sialkot, Sialkot, PK-PB 51310, PK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Laryngeal Injection Set EMERGENCY, CARDIOPULMONARY Ophthalmoscope Battery Powered Tuning Fork Laryngoscope Examination Light Tongue Depressor Laryngoscope Blade Laryngoscope Handle Otoscope STETHOSCOPE, MANUAL specula Examination Light Accessories HAMMER, SURGICAL Probe ENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KAA	Set, Laryngeal Injection	Ear, Nose, Throat	Class 1	874.4420	2026-03-05
BZN	Cart, Emergency, Cardiopulmonary (Excluding Equipment)	Anesthesiology	Class 1	868.6175	2026-03-05
HLJ	Ophthalmoscope, Battery-Powered	Ophthalmic	Class 2	886.1570	2026-03-05
GWX	Fork, Tuning	Neurology	Class 1	882.1525	2026-03-05
EQL	Laryngostroboscope	Ear, Nose, Throat	Class 1	874.4750	2026-03-05
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2026-03-05
KBL	Depressor, Metal Tongue, Surgical	Ear, Nose, Throat	Class 1	874.4420	2026-03-05
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2026-03-05
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2026-03-05
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2026-03-05
HNC	Specula, Ophthalmic	Ophthalmic	Class 1	886.4350	2026-03-05
PEQ	Accessories To Examination Light	General Hospital	Class 1	880.6320	2026-03-05
FZY	Hammer, Surgical	General, Plastic Surgery	Class 1	878.4800	2026-03-05
KAK	Probe, Ent	Ear, Nose, Throat	Class 1	874.4420	2026-03-05

Official Correspondent

Abdul Jabbar

US Agent Details

CHAD CAPPIELLO Business: QA International Email: moazmaqai@gmail.com Phone: (908) 3094967

Related Public Records

Same Entity

Doctor Devices

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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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9611102	RICHARD WOLF GMBH	KNITTLINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027187888. Last updated year: 2026. Please use registration number 3027187888 when referencing this establishment in official correspondence.