MEKICS CO., LTD.

FDA Device Registration & Listing · Paju-si Gyeonggi, KR · Registration 3013190994

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
3013190994
FEI Number
3013190994
Entity Name
MEKICS CO., LTD.
City/State/Country
Paju-si Gyeonggi, KR
Establishment Address
21, Sangjiseok-gil, Paju-si Gyeonggi 10911, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MEKICS Co., Ltd. (Owner Number: 10094795)
Owner / Operator Contact Address
21, Sangjiseok-gil, Paju-si, KR-41 10911, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

HFT750U

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MNT Sv70 Ventilator Anesthesiology Class 2 868.5895 2026-01-05

Official Correspondent

SangHag Lee

US Agent Details

Matt Dryden Email: matt.dryden@promedic.cc Phone: (239) 3076061

Related Public Records

Same Entity

MEKICS Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013190994. Last updated year: 2026. Please use registration number 3013190994 when referencing this establishment in official correspondence.
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