PZMEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Putuo District Shanghai, CN · Registration 3013688559

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
3013688559
FEI Number
3013688559
Entity Name
PZMEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Putuo District Shanghai, CN
Establishment Address
5F, Building 13, No. 2 Suide Road, Putuo District Shanghai 200331, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PZMedical Technology Co., Ltd. (Owner Number: 10055327)
Owner / Operator Contact Address
5F, Building 13, No. 2 Suide Road, Putuo District, CN-SH 200331, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K170480
PMA Number
N/A

All Registered Proprietary Names

Model 4343A Model 2929A Model A843B Model 3543A

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2017-07-07

Official Correspondent

No official correspondent registered.

US Agent Details

Daniel Kamm Business: Kamm & Associates Email: fda.help.now@gmail.com Phone: (847) 3741727

Related Public Records

Same Entity

PZMedical Technology 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
K070563 Vidar Systems Corp. VIDAR VISION 2000 2007-03-16
K190691 Pixxgen Corporation Pixx2430 Digital Diagnostic X-Ray Receptor Panel 2019-04-04
K150150 Rayence Co., Ltd. 1717SGN / 1717SCN Digital Flat Panel X-ray Detector 2015-03-27
K140771 Philips Medical Systems Dmc GmbH PHILIPS ELEVA WORKSPOT 2014-04-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2009 Toshiba American Medical Systems Inc 2
Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography System with version 3.40 or higher software. Controller for Infinix interventional angiography systems.
Z-0031-2007 AGFA Corp. 2
CR DX-S, Image Intensified Fluoroscopic X-ray system.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013688559. Last updated year: 2026. Please use registration number 3013688559 when referencing this establishment in official correspondence.
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