Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017265430

FEI Number

3017265430

Entity Name

SHENZHEN YOUMAY ELECTRONICS CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Room 208 Minyue Technology Building, Minzhi Street, Longhua District, Shenzhen Guangdong 518000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Youmay Electronics Co., Ltd (Owner Number: 10073424)

Owner / Operator Contact Address

Room 208 Minyue Technology Building, Minzhi Street, Longhua District, Shenzhen, CN-GD 518000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UNIT, HEATING, POWERED DEVICE, PRESSURE APPLYING HUMIDIFIER, NON-DIRECT PATIENT INTERFACE (HOME-USE) Massager, therapeutic, electric Respirator, surgical Face Mask Within the Scope of the Face Mask and Barrier Face Covering Enforcement Policy or Face Mask Umbrella EUA TOOTHBRUSH, POWERED Lamp, surgical SCALE, STAND-ON, PATIENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IRQ	Unit, Heating, Powered	Physical Medicine	Class 1	890.5950	2023-04-02
KNM	Device, Pressure Applying	Physical Medicine	Class 1	890.5765	2023-06-16
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2023-06-16
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2021-04-26
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2020-05-09
QKR	Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua	Unknown	Class N	N/A	2020-05-09
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2023-06-16
FTD	Lamp, Surgical	General, Plastic Surgery	Class 2	878.4580	2023-06-16
FRI	Scale, Stand-On, Patient	General Hospital	Class 1	880.2700	2023-04-02

Official Correspondent

Peng Liao

US Agent Details

Cindy Wu Business: HOORAY INDUSTRY LLC Email: AmbertFDA@outlook.com Phone: (626) 9105808

Related Public Records

Same Entity

Shenzhen Youmay Electronics 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
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

Similar Registrations

Registration Number	Establishment Name	Location
3010227982	Tianjin Zhengtian Medical Instrument Co., Ltd.	Tianjin, CN
8010177	STRYKER LEIBINGER GMBH & CO. KG	FREIBURG Baden-Wurttemberg, DE
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE
3018448099	HANIL MEDICAL CO., LTD.	Gwangju-si, KR
3011066654	SHENZHEN JOOSE BEAUTY ELECTRONIC CO.,LTD	Shen Zhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017265430. Last updated year: 2026. Please use registration number 3017265430 when referencing this establishment in official correspondence.