Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006113277

FEI Number

3006113277

Entity Name

WENZHOU LONGWAN MEDICAL DEVICE FACTORY

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

Unit 4, Building 27, No. 706 Yanyun Road, Oujiangkou Industrial Cluster District, Wenzhou Zhejiang 325026, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Wenzhou Longwan Medical Device Factory (Owner Number: 10062272)

Owner / Operator Contact Address

Unit 4, Building 27, No. 706 Yanyun Road, Oujiangkou Industrial Cluster District, Wenzhou, CN-ZJ 325026, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer Tourniquet BOTTLE, HOT/COLD WATER BLOOD PRESSURE CUFF INFUSOR, PRESSURE, FOR I.V. BAGS Percussion Hammer OTOSCOPE penlight Stethoscope SCISSORS, MEDICAL, DISPOSABLE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2024-03-22
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2024-03-22
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2020-12-17
FPF	Bottle, Hot/Cold Water	General Hospital	Class 1	880.6085	2023-12-21
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2022-06-20
KZD	Infusor, Pressure, For I.V. Bags	General Hospital	Class 1	880.5420	2023-12-21
FZY	Hammer, Surgical	General, Plastic Surgery	Class 1	878.4800	2020-12-17
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2023-12-21
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2020-12-17
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2020-01-07
JOK	Scissors, Medical, Disposable	General Hospital	Class 1	880.6820	2023-12-21

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Business: Medright Tech Inc Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

Wenzhou Longwan Medical Device Factory

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

Similar Registrations

Registration Number	Establishment Name	Location
3031192529	Zhejiang LuDe Technology Development Co., Ltd.	Wenzhou Zhejiang, CN
3002865611	BALLERSTEDT GMBH	Reinbek Schleswig-Holstein, DE
3009154535	WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD.	Wenzhou City Zhejiang, CN
1058002	Technicuff Corp.	LEESBURG, FL, US
3001570235	GE Medical Systems Information Technologies, Inc.	Waukesha, WI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006113277. Last updated year: 2026. Please use registration number 3006113277 when referencing this establishment in official correspondence.