Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9680874

FEI Number

3000953362

Entity Name

MDF Instruments Medifriend Inc.

City/State/Country

SONG JIANG DISTRICT, SHANGHAI, CN

Establishment Address

1898 LAI YIN RD, BLDG 6, 3F / BLDG 2, 1F, JIU TING TOWN, SONG JIANG DISTRICT, SHANGHAI 201615, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MDF Instruments Medifriend Inc. (Owner Number: 9012076)

Owner / Operator Contact Address

1898 LAI YIN RD, BLDG 6, 3F / BLDG 2, 1F, JIU TING TOWN, SONG JIANG DISTRICT, SHANGHAI, CN-SH 201615, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Oral Screw BATTERY POWERED GENERAL HOSPITAL LIGHT EXAMINATION VARIOUS MODEL SURGICAL NONPNEUMATIC GENERAL AND PLASTIC S URGERY RULERS AND CALIPERS GENERAL AND PL ASTIC SURGERY MDF® Mobile Aneroid Sphyg MDF® Desk Mercury Sphygmomanometer MDF® Medic Palm¿ Aneroid Sphyg MDF® Desk & Wall Aneroid Sphyg MDF® Professional Aneroid Sphyg MDF® Calibra Pro Aneroid Sphygmomanometer Snellen Pocket Eye Chart Tongue Depressor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KBW	Screw, Oral	Ear, Nose, Throat	Class 1	874.4420	2008-02-28
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2006-03-13
KDC	Instrument, Surgical, Disposable	General, Plastic Surgery	Class 1	878.4800	1994-12-12
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2006-03-13
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2006-03-13
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2007-11-30
HOX	Chart, Visual Acuity	Ophthalmic	Class 1	886.1150	2022-01-13
FMA	Depressor, Tongue, Non-Surgical	General Hospital	Class 1	880.6230	1994-12-12

Official Correspondent

Helen Wu

US Agent Details

Elmer Mendez Business: MDF Instruments Direct, Inc. Email: admin@medifriend.com Phone: (818) 3575647

Related Public Records

Same Entity

MDF Instruments Medifriend Inc.

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
K831798	I M, Inc.	DISPOSABLE SCALPELS	1983-07-19
K831001	Frontier Products	UNICUFF-BLOOD PRESSURE CUFF	1983-07-28
K253089	Shenzhen Best Electronics Co., Ltd.	NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)	2026-02-13
K972301	Rudolf Riester GmbH & Co. KG	BIG BEN SQUARE, BIG BEN ROUND	1997-09-17

Similar Registrations

Registration Number	Establishment Name	Location
8010733	PRO-MED INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
8040278	Falcon Surgical Co. (Pvt.) Ltd.	Sialkot Punjab, PK
3003418325	Integra LifeSciences Corporation	Princeton, NJ, US
1836161	ASPEN SURGICAL PRODUCTS, INC.	Caledonia, MI, US
3006061749	FLEXICARE MEDICAL (DONGGUAN) LTD.	DONGGUAN CITY Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680874. Last updated year: 2026. Please use registration number 9680874 when referencing this establishment in official correspondence.