Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033881629

FEI Number

3033881629

Entity Name

Ansion Technology (GuangDong) Co., Ltd.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Room 302,Building 2,No.2 Kunming Road, Liaobu Town, Dongguan Guangdong 523000, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Ansion Technology (GuangDong) Co. Ltd. (Owner Number: 10091823)

Owner / Operator Contact Address

Room 302,Building 2,No.2 Kunming Road, Liaobu Town, Dongguan, CN-GD 523000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AVCOO, 3 in 1 TENS UNIT, model TS2301 AVCOO, 3 in 1 TENS UNIT, model TS2321 AUVON, Tens & Ems Device, model TU1080 AUVON, TENS and EMS Unit, model TC3241

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2025-09-15
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2025-09-15
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2025-07-30
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2025-07-30
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2026-01-14
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2026-01-14

Official Correspondent

Jack Tan

US Agent Details

Simin Lin Email: simin_lin123@126.com Phone: (415) 6026843

Related Public Records

Same Entity

Ansion Technology (GuangDong) 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
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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3013889849	Expeditors International of Washington, Inc.	Salt Lake City, UT, US
3044675848	PEPPER INTERACTIVE INC	Wilmington, DE, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033881629. Last updated year: 2026. Please use registration number 3033881629 when referencing this establishment in official correspondence.