Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022764539

FEI Number

3022764539

Entity Name

LUCA AICELL

City/State/Country

Anyang-si Gyeonggi, KR

Establishment Address

3rd floor, 11-35, Simin-daero 327beon-gil, Dongan-gu, Anyang-si Gyeonggi 14055, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LUCA AICell (Owner Number: 10085130)

Owner / Operator Contact Address

3rd floor, 11-35, Simin-daero 327beon-gil, Dongan-gu, Anyang-si, KR-41 14055, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LUCA Allergy Nasal Spray, NOSEBREEZE, NOSE MEDIC ALLERGIC NASAL SPRAY LUCA V-Defense Nasal Spray, VD99 Nasal Spray, NS01-20LF, Coepic nose barrier 99.7 LUCA Allergy Nasal Spray Q Plus SKINTACT (Model: MD01-01D)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2023-01-08
NEC	Bandage, Liquid, Skin Protectant	General Hospital	Class 1	880.5090	2024-06-28

Official Correspondent

Taehoon Kim

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

LUCA AICell

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 3022764539. Last updated year: 2026. Please use registration number 3022764539 when referencing this establishment in official correspondence.