Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011221272

FEI Number

3011221272

Entity Name

MSLINE ENG CO LTD

City/State/Country

Icheon-si Gyeonggi, KR

Establishment Address

26, Wonjeok-ro 148 beon-gil, Sindun-myeon, Icheon-si Gyeonggi 17302, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MSLINE ENG Co Ltd (Owner Number: 10047485)

Owner / Operator Contact Address

26, Wonjeok-ro 148 beon-gil, Sindun-myeon, Icheon, KR-41 17302, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Manual Collimator (Model: Radsafe)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EAK	Screen, Leaded, Operator Radiation Protector	Radiology	Class 1	892.6500	2014-09-16

Official Correspondent

Jae-Sang Ham

US Agent Details

JR Kimt Business: Meddatcom Email: meddatcom@gmail.com Phone: (732) 2591690

Related Public Records

Same Entity

MSLINE ENG 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 3011221272. Last updated year: 2026. Please use registration number 3011221272 when referencing this establishment in official correspondence.