MEDICAPS CO., LTD.

FDA Device Registration & Listing · Seongnam-si Gyeonggi, KR · Registration 3026391023

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
3026391023
FEI Number
3026391023
Entity Name
MEDICAPS CO., LTD.
City/State/Country
Seongnam-si Gyeonggi, KR
Establishment Address
202-ho, New Seonkyung Plaza,, 13 Imae-ro, Bundang-gu,, Seongnam-si Gyeonggi 13564, KR
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Medicaps Co., Ltd (Owner Number: 10092335)
Owner / Operator Contact Address
10, Bundang-ro 53beon-gil, Bundang-gu,, Seongnam-si, KR-41 13591, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Philips Brilliance CT Parts for Brilliance iCT 256 GE Discovery 690 PET/CT Philips Allura FD20 Siemens Artis Zee Cath Angio GE Discovery MR750

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JAK System, X-Ray, Tomography, Computed Radiology Class 2 892.1750 2025-01-02
JAY Support, Breathing Tube Anesthesiology Class 1 868.5280 2024-12-24
KPS System, Tomography, Computed, Emission Radiology Class 2 892.1200 2026-03-01
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2025-07-08
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2025-07-08
IZI System, X-Ray, Angiographic Radiology Class 2 892.1600 2025-07-08
IZI System, X-Ray, Angiographic Radiology Class 2 892.1600 2026-03-19
LNH System, Nuclear Magnetic Resonance Imaging Radiology Class 2 892.1000 2025-06-20

Official Correspondent

Kenny Kim

US Agent Details

Grace Lyon Business: Block Imaging Parts and Service Email: grace.lyon@blockimaging.com Phone: (517) 6688800

Related Public Records

Same Entity

Medicaps 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
K243523 Siemens Medical Solutions USA, Inc. NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime 2025-02-12
K781431 General Electric Co. ELECTRIC CT/T OPERATOR DISPLAY CONSOLE 1978-09-07
K231574 FUJIFILM Healthcare Americas Corporation Scenaria View 4.2 2023-10-12
K233583 FUJIFILM Healthcare Americas Corporation FCT iSTREAM Phase 1 2024-04-26
K151376 Covidien, LLC superDimension Navigation System 2015-11-05

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0007-2011 GE Medical Systems, LLC 2
HiSpeed X/i Computed Tomography operator consoles with the Model Number 2153675 and 2247802. The expected usage of this product is to generate head and whole body CT images of human subjects.
Z-0009-2017 Philips Medical Systems 2
Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Z-0010-2017 Philips Medical Systems 2
Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Z-0011-2017 Philips Medical Systems 2
Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Z-0012-2017 Philips Medical Systems 2
Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026391023. Last updated year: 2026. Please use registration number 3026391023 when referencing this establishment in official correspondence.
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