Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034397208

FEI Number

3034397208

Entity Name

HONG KONG LANLI TECHNOLOGY CO., LIMITED

City/State/Country

TUEN MUN, HK

Establishment Address

SHOP 185 G/F, HANG WAI IND. CENTRE, NO.6 KIN TAI ST., TUEN MUN 999077, HK

Establishment Type(s)

Repack or Relabel Medical Device,Remanufacture Medical Device

Owner / Operator

Hong Kong Lanli Technology Co., Limited (Owner Number: 10092134)

Owner / Operator Contact Address

SHOP 185 G/F, HANG WAI IND. CENTRE, NO.6 KIN TAI ST., TUEN MUN, HK-NOTA 999077, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K823319

PMA Number

N/A

All Registered Proprietary Names

Personal Steam Inhaler, Vocal Steamer for Sinus Relief, Allergies, Congestion & Colds Plaque Remover for Teeth, Electric Tartar Remover (BCM197) Plaque Remover for Teeth, Electric Tartar Remover for Teeth

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	2026-05-19
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2026-03-25
EMS	Curette, Periodontic	Dental	Class 1	872.4565	2026-04-21

Official Correspondent

XING HUANG

US Agent Details

JACLINE BOBOIGE Email: boboigechen@gmail.com Phone: (414) 9442888

Related Public Records

Same Entity

Hong Kong Lanli Technology Co., Limited

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 3034397208. Last updated year: 2026. Please use registration number 3034397208 when referencing this establishment in official correspondence.