Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012373810

FEI Number

3012373810

Entity Name

AUO (SUZHOU) CO., LTD.

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

No. 398, Suhong Zhong Road, Suzhou Industrial Park, 215021, China, Suzhou Jiangsu 215021, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

AUO (Suzhou) Co., Ltd. (Owner Number: 10091604)

Owner / Operator Contact Address

No. 398, Suhong Zhong Road, Suzhou Industrial Park, 215021, China, Suzhou, CN-JS 215021, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MH2441A; MH2441A-E; MH2441A-J; MH2441A-P; MH2441A-R; MH2441A-W; MH2441AY; MH2441AZ; MH2741A; MH2741A-E; MH2741A-J; MH2741A-P; MH2741A-R; MH2741A-W; MH2741AY; MH2741AZ;

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LMD	System, Digital Image Communications, Radiological	Radiology	Class 1	892.2020	2024-11-14

Official Correspondent

Bruce Chen

US Agent Details

Simon Nip Email: simon.nip@auodplus.com Phone: (617) 6787359

Related Public Records

Same Entity

AUO (Suzhou) 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 3012373810. Last updated year: 2026. Please use registration number 3012373810 when referencing this establishment in official correspondence.