FOSHAN GAUNYING ELECTRONICS CO., LTD

FDA Device Registration & Listing · Foshan Guangdong, CN · Registration 3008395118

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008395118
FEI Number
3008395118
Entity Name
FOSHAN GAUNYING ELECTRONICS CO., LTD
City/State/Country
Foshan Guangdong, CN
Establishment Address
No. 501, 5th Floor, Building 5, No. 51, Jiang Hai Road, Zhang Cha Street, Chan Cheng District, Foshan Guangdong 528000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Foshan Gaunying Electronics Co., LTD (Owner Number: 10032493)
Owner / Operator Contact Address
No. 501, 5th Floor, Building 5, No. 51, Jiang Hai Road,, Zhang Cha Street, Chan Cheng District, Foshan, CN-GD 528000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K121154
PMA Number
N/A

All Registered Proprietary Names

Gaunying Infrared Lamp FIR51, SN-51

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2014-01-29
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2011-07-15
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2011-07-13
KFZ Humidifier, Non-Direct Patient Interface (Home-Use) Anesthesiology Class 1 868.5460 2014-01-29
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2013-08-30

Official Correspondent

Charles Shen

US Agent Details

Charles Shen Business: Manton Business and Technology Services Email: cyshen@aol.com Phone: (608) 2179358

Related Public Records

Same Entity

Foshan Gaunying 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
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07

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3005998497 SUNMED AP, LTD. ZHUHAI Guangdong, CN
3006852037 Omron Healthcare Manufacturing Vietnam Co., Ltd. Ho Chi Minh City, VN
3006783791 GaleMed (Xiamen) Co., Ltd. XIAMEN Fujian, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008395118. Last updated year: 2026. Please use registration number 3008395118 when referencing this establishment in official correspondence.
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