Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033524192

FEI Number

3033524192

Entity Name

Noul Co., Ltd.

City/State/Country

Yongin Si Gyeonggi, KR

Establishment Address

B-6,10F, 338, Gwanggyojungang-ro, Suji-gu, Yongin Si Gyeonggi 16942, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Noul Co., Ltd. (Owner Number: 10091889)

Owner / Operator Contact Address

B-6,10F, 338, Gwanggyojungang-ro, Suji-gu, Yongin Si, KR-41 16942, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SafeFix SafeFix CER miLab Platform miLab Platform

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LDZ	Fixative, Alcohol Containing	Pathology	Class 1	864.4010	2024-11-13
KEM	Agent, Clearing	Pathology	Class 1	864.4010	2025-09-16
IBJ	Light, Microscope	Pathology	Class 1	864.3600	2024-11-17
KPA	Slide Stainer, Automated	Pathology	Class 1	864.3800	2024-11-17

Official Correspondent

Chan-yang Lim

US Agent Details

Peter Kim Business: MSEED, INC Email: peter@noul.com Phone: (310) 7440493

Related Public Records

Same Entity

Noul 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
K761138	Zeus Scientific, Inc.	FA TISSUE FIXATIVE & WASH SET	1978-01-06
K842913	E K Ind., Inc.	WRIGHT STAIN FIXATIVE	1984-09-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033524192. Last updated year: 2026. Please use registration number 3033524192 when referencing this establishment in official correspondence.