BEIJING KONTED MEDICAL TECHNOLOGY CO., LTD

FDA Device Registration & Listing · Beijing, CN · Registration 3027501622

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
3027501622
FEI Number
3027501622
Entity Name
BEIJING KONTED MEDICAL TECHNOLOGY CO., LTD
City/State/Country
Beijing, CN
Establishment Address
Room 111,1F, No. 27, Yong wang Road, Daxing Biological, Building 3, Pharmaceutical Industry Base, Daxing District, Beijing 102629, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Beijing Konted Medical Technology Co., Ltd (Owner Number: 10089936)
Owner / Operator Contact Address
Room 111,1F, Building 3, No. 27, Yong wang Road, Daxing Biological, Pharmaceutical Industry Base, Daxing District, Beijing, CN-NOTA 102629, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pocket Ultrasound System (Model: C10, C10HL, C10XL, C10XLpro, C10RC, C10HQ, C10CW, C10UC) Portable Vein Finder

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IYN System, Imaging, Pulsed Doppler, Ultrasonic Radiology Class 2 892.1550 2024-01-24
ITX Transducer, Ultrasonic, Diagnostic Radiology Class 2 892.1570 2024-01-24
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2024-01-24
KZA Device, Vein Location, Liquid Crystal General Hospital Class 1 880.6970 2026-02-11

Official Correspondent

Deyi Zhu

US Agent Details

Faye Liang Business: SHARE INFO INC. Email: cfrhealthcare@foxmail.com Phone: (929) 4102964

Related Public Records

Same Entity

Beijing Konted Medical 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
K191007 Supersonic Imagine Aixplorer MACH 30, Aixplorer MACH 20 Ultrasound Diagnostic Systems 2019-10-25
K974588 Rimed , Ltd. INTRA-VIEW BILATERAL TRANSCRANIAL DOPPLER DEVICE, SMART-LITE PORTABLE BILATERAL TRANSCRANIAL DOPPLER DEVICE, COMPACT MOD 1998-08-07
K142628 Siemens Medi Cal Solutions, Inc. Acuson SC2000 Diagnostic Ultrasound System 2014-10-10
K132171 Supersonic Imagine AIXPLORER 2013-09-24
K222441 Bk Medical Aps Ultrasound System 2300 2022-12-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0189-2022 FujiFilm Healthcare Americas Corporation 2
Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3
Z-0190-2022 FujiFilm Healthcare Americas Corporation 2
Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
Z-0191-2022 FujiFilm Healthcare Americas Corporation 2
Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3
Z-0192-2022 FujiFilm Healthcare Americas Corporation 2
Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0
Z-1884-2024 FUJIFILM Healthcare Americas Corporation 2
Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027501622. Last updated year: 2026. Please use registration number 3027501622 when referencing this establishment in official correspondence.
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