Guangzhou Telefield Limited

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3013494333

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
3013494333
FEI Number
3013494333
Entity Name
Guangzhou Telefield Limited
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
No.11 Guang Cong Sixth Road, First Industrial Zone, Zhuliao, Guangzhou Baiyun Area, Guangdong Province, P.R. China, Guangzhou Guangdong 510545, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Guangzhou Telefield Limited (Owner Number: 10057382)
Owner / Operator Contact Address
No. 11, Guang Cong Sixth Road, First Industrial Zone, ZhuLiao, GuangZhou BaiYun Area,, GuangZhou, CN-GD 510545, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CAN Go

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect General, Plastic Surgery Class 2 878.4810 2018-03-27
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2018-03-27
KHY Cane, Safety Walk Physical Medicine Class 1 890.3075 2021-12-17

Official Correspondent

Florence Lee

US Agent Details

Michelle Lott Business: Principal Email: michelle@leanraqa.com Phone: (520) 2759838

Related Public Records

Same Entity

Guangzhou Telefield Limited
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
K192521 Shangdong Huamei Technology Co., Ltd. Intense Pulsed Light Treatment System 2019-12-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013494333. Last updated year: 2026. Please use registration number 3013494333 when referencing this establishment in official correspondence.
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