Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021082429

FEI Number

3021082429

Entity Name

MEDIFAB CO., LTD.

City/State/Country

Geumcheon-gu Seoul, KR

Establishment Address

#B222, #415~418, Daeryung Techno Town 20 Cha, 5 Gasan digital 1-ro,, Geumcheon-gu Seoul 08594, KR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

MediFab Co., Ltd. (Owner Number: 10083484)

Owner / Operator Contact Address

#B222, #415~418, Daeryung Techno Town 20 Cha, 5 Gasan digital 1-ro, Geumcheon-gu, KR-11 08594, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RES NOVAE CORE IMPACT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2024-07-17

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

MediFab 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 3021082429. Last updated year: 2026. Please use registration number 3021082429 when referencing this establishment in official correspondence.