TIA

FDA Device Registration & Listing · Gimje-si Jeonbuk, KR · Registration 3017405990

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
3017405990
FEI Number
3017405990
Entity Name
TIA
City/State/Country
Gimje-si Jeonbuk, KR
Establishment Address
20, Daedonggongdan 2-gil, Mangyeong-eup, Gimje-si Jeonbuk 54325, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TIA (Owner Number: 10080145)
Owner / Operator Contact Address
20, Daedonggongdan 2-gil, Mangyeong-eup, Gimje-si, KR-45 54325, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BOTN Prevention of Epidemic Mask(KF94) BOTN Natural 2D Style Mask(KF94)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2021-01-14
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2022-10-07

Official Correspondent

Chang Soo Kim

US Agent Details

Sunyoung Park Email: sypark@szukorea.com Phone: (682) 7729233

Related Public Records

Same Entity

TIA
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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017405990. Last updated year: 2026. Please use registration number 3017405990 when referencing this establishment in official correspondence.
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