Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016872092

FEI Number

3016872092

Entity Name

WENZHOU ZUOYOU MEDICAL TECHNOLOYG CO.,LTD.

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

Puqi Industrial Zone,Puqi Town,Yueqing City (Inside Yueqing Baofeng Plastic And Electric Co.,Ltd.), Wenzhou Zhejiang 325608, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Wenzhou Zuoyou Medical Technoloyg Co.,Ltd. (Owner Number: 10067521)

Owner / Operator Contact Address

Puqi Industrial Zone,Puqi Town,Yueqing City (Inside Yueqing Baofeng Plastic And Electric Co.,Ltd.), Wenzhou, CN-ZJ 325608, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Self-adhesive bandage Electric Toothbrush,Sonic Toothbrush CR-8105 Rotating electric toothbrush LittleSmiles,CR-8201,CR-8202,CR-8203,CR-8204,CR-8205,CR-8101,CR-8102,CR-8103,CR-8104 U-shaped children's electric toothbrush, LittleSmiles U-shaped children's electric toothbrush, nasal wash CR-7100, CR-7110 nasal washer,nasal wash bottle,Nasal irrigator,Sinus irrigator oral irrigator, Powered Nasal - Electric Nasal Irrigation,Sinus cleaner Douche Apparatus Toothbrush UV Sterilizer Oral Irrigation Toothbrush Nasal Spray,Spray bottle, Saline Nasal Wash, Saline nasal spray, Seawater nasal spray, Nasal clean stoma bag disposable diapers ear cleaner Ear washer Body Wash Bottle ED300 Vaginal irrigator,Woman washer Woman washer bidet,PERSONAL HYGIENE CARE,vaginal cleaner,Vaginal Douche PORTABLE BIDET,POSTPARTUM CARE,Vaginal Cleansing System,Syringe, Irrigating (Non Dental) Sunscreen mask kneepad bandage, Band-aid Cupping

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2024-12-30
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2020-04-05
KMA	Irrigator, Powered Nasal	Ear, Nose, Throat	Class 1	874.5550	2020-04-05
HED	Douche Apparatus, Vaginal, Therapeutic	Obstetrics/Gynecology	Class 1	884.5900	2020-04-26
NOB	Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile	Dental	Class 1	872.6855	2022-04-08
OGT	Oral Irrigation Kit	Dental	Class 1	872.6510	2020-04-05
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2020-04-05
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2020-04-05
EXB	Collector, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2020-04-05
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2024-12-30
OGQ	Ear Irrigation Kit	General Hospital	Class 1	880.6960	2020-04-05
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2020-04-05
KPY	Shield, Protective, Personnel	Radiology	Class 1	892.6500	2024-12-30
ITQ	Joint, Knee, External Brace	Physical Medicine	Class 1	890.3475	2024-12-30
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2024-12-30
KNM	Device, Pressure Applying	Physical Medicine	Class 1	890.5765	2024-12-30

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 Zuoyou Medical Technoloyg Co.,Ltd.

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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2012	Convatec Inc.	1	Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System (57 mm) Required for application to a patient immediately after ostomy surgery.

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3012453673	FANNIN (UK) LIMITED	Measham, Swadlincote Derbyshire, GB
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016872092. Last updated year: 2026. Please use registration number 3016872092 when referencing this establishment in official correspondence.