SAMSUNG ELECTRONICS CO., LTD.

FDA Device Registration & Listing · Seoul, KR · Registration 3032116890

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
3032116890
FEI Number
3032116890
Entity Name
SAMSUNG ELECTRONICS CO., LTD.
City/State/Country
Seoul, KR
Establishment Address
1077, Cheonho-daero, Gangdong-gu, Seoul 05340, KR
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Samsung Electronics Co., Ltd. (Owner Number: 10043488)
Owner / Operator Contact Address
129, Samsung-ro, Yeongtong-gu, Suwon-si, KR-41 16677, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

AccE GM85; GM85; GM85 with Lite; GM85 with Prestige: GM85 Elite AccE GM85; GM85; GM85 with Lite; GM85 with Prestige GR40CW; GM85 GC85A AccE GM85; GM85; GM85 with Lite; GM85 with Prestige GF85 GF85-3P AccE GF85 GF85-SP GC85A GM85 AccE GM85; GM85; GM85 with Lite; GM85 with Prestige GR40CW; S4335-WV ALND; Auto Lung Nodule Detection GR40CW; GM85; GC85A GR40CW; S4335-W; XGEO GR40CW

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2024-11-20
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2022-04-25
KPR System, X-Ray, Stationary Radiology Class 2 892.1680 2018-05-24
KPR System, X-Ray, Stationary Radiology Class 2 892.1680 2016-07-21
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2018-07-25
KPR System, X-Ray, Stationary Radiology Class 2 892.1680 2024-09-23
KPR System, X-Ray, Stationary Radiology Class 2 892.1680 2015-04-05
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2016-11-15
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2016-11-15
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2022-10-11
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2015-12-21
MYN Analyzer, Medical Image Radiology Class 2 892.2070 2021-09-02
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2018-12-09
KPR System, X-Ray, Stationary Radiology Class 2 892.1680 2018-12-09
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2018-12-09
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2014-06-02

Official Correspondent

Sangkyun Kang

US Agent Details

Ninad Gujar Business: Samsung HME America, Inc. Email: ngujar@neurologica.com Phone: (978) 5648632

Related Public Records

Same Entity

Samsung Electronics Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004938766 Samsung HME America, Inc. Danvers, MA, US
3017616353 Samsung Electronics Co., Ltd. Mobile eXperience Business Suwon-si Gyeonggi, KR
3010300212 Samsung Electronics Co., Ltd. Suwon-si Gyeonggi, KR

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K123106 Samsung Electronics Co., Ltd. DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A 2013-06-20
K153059 Minxray, Inc. HF1202H PowerPlus Portable X-ray Equipment 2016-02-02
K201670 Siemens Medical Solutions USA, Inc. YSIO X.pree 2020-10-21
K203340 Siemens Medical Solutions USA, Inc. MULTIX Impact C 2021-01-06
K230241 Sg Healthcare Co, Ltd. Jumong General 2023-02-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-1470-2023 FUJIFILM Healthcare Americas Corporation 2
FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams
Z-3158-2024 FUJIFILM Healthcare Americas Corporation 2
The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.
Z-0002-2009 GE Medical Systems, LLC 2
Revolution XR/d system control room PC model 5117866-2 with Software collector 5115434
Z-0002-2015 Siemens Medical Solutions USA, Inc 2
Siemens Ysio Max system The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and bariatric patients. It can also be used for intravenous, small interventions (like biopsy, punctures, etc.) and emergency (trauma, critical ill) applications. Exposures may be taken with the patient sitting, standing, or in the prone position. The Ysio Max system is not meant for mammography. The Ysio Max uses integrated or portable digital detectors for generating diagnostic images by converting x-rays into electronic signals. Ysio Max is also designed to be used with conventional film/screen or Computed Radiography (CR) cassettes.
Z-0003-2009 GE Medical Systems, LLC 2
Revolution XR/d systems with control room PC model 5117866-2 with Software collector 5194381. GE Healthcare, 3000 North Grandview, Waukesha, WI 53188. Intended for use in generating Tomographic images of human anatomy.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032116890. Last updated year: 2026. Please use registration number 3032116890 when referencing this establishment in official correspondence.
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