Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029915531

FEI Number

3029915531

Entity Name

RHINOCARE KOREA INC.

City/State/Country

Gumi-si Gyeongbuk, KR

Establishment Address

#307, #303, 253, Sanho-daero, Gumi-si Gyeongbuk 38371, KR

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

RhinoCare Korea Inc. (Owner Number: 10088929)

Owner / Operator Contact Address

#307, #303, 253, Sanho-daero, Gumi-si, KR-47 38371, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RC-N11F therapeutic humidifier for home use RC-N23E therapeutic humidifier for home use

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2023-10-23

Official Correspondent

Hye Yeon Choi

US Agent Details

Dave Kim Business: Mtech Group LLC Email: davekim@mtechgroupllc.com Phone: (713) 4672607

Related Public Records

Same Entity

RhinoCare Korea Inc.

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 3029915531. Last updated year: 2026. Please use registration number 3029915531 when referencing this establishment in official correspondence.