Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027641448

FEI Number

3027641448

Entity Name

GoldenHour Co., LTd.

City/State/Country

Cheongju-si Chungbuk, KR

Establishment Address

Chungbuk National University G-Tech Venture Center, 1251, Garosu-ro, Heungdeok-gu, main building-Room 301-2, 3rd floor, Bokdae-dong, Cheongju-si Chungbuk 28420, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GoldenHour Co.,LTd (Owner Number: 10088406)

Owner / Operator Contact Address

Chungbuk National University G-Tech Venture Center, 1251, Garosu-ro, Heungdeok-gu, main building-Room 301-2, 3rd floor, Bokdae-dong, Cheongju-si, KR-43 28420, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Air Capsule [Bump type / General type]

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2023-07-17

Official Correspondent

DAE JONG KIM

US Agent Details

David Hyun Jun Paek Email: dpaek.rennes@gmail.com Phone: (818) 9030660

Related Public Records

Same Entity

GoldenHour 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 3027641448. Last updated year: 2026. Please use registration number 3027641448 when referencing this establishment in official correspondence.