Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015447513

FEI Number

3015447513

Entity Name

LINX (ASIA) TRADING CO., LTD

City/State/Country

Dongguan Guangdong, CN

Establishment Address

RM 702, Building 32, Golden Town, Keji Rd, Houjie, Dongguan Guangdong 523945, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Linx (Asia) Trading Co., Ltd (Owner Number: 10050141)

Owner / Operator Contact Address

RM 702, Building 32, Golden Town, Keji Rd, Houjie,, Dongguan, CN-GD 523945, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EXQ	Cystometer, Electrical Recording	Gastroenterology, Urology	Class 2	876.1620	2020-08-23

Official Correspondent

Justin Tian

US Agent Details

Richard Hart Richard Hart Email: rhart@srsmedical.com Phone: (978) 6632800

Related Public Records

Same Entity

Linx (Asia) Trading Co., Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015447513. Last updated year: 2026. Please use registration number 3015447513 when referencing this establishment in official correspondence.