Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012219816

FEI Number

3012219816

Entity Name

FAIRFORM MFG., CO., LTD

City/State/Country

HONG KONG, HK

Establishment Address

Suite 1909B, 19/F,Tower 3,China Hong Kong City, 33 Canton Road, Tsim Sha Tsui, Kowloon,, HONG KONG HK-NA, HK

Establishment Type(s)

Foreign Private Label Distributor,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

FAIRFORM MFG., CO., LTD (Owner Number: 10054901)

Owner / Operator Contact Address

Suite 1909B, 19/F,Tower 3, China Hong Kong City, 33 Canton Road, Tsim Sha Tsui, Kowloon, HONG KONG, HK-NOTA HK-NA, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMD	Toothbrush, Ionic, Battery-Powered	Dental	Class 1	872.6865	2017-12-06
NOB	Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile	Dental	Class 1	872.6855	2021-11-30

Official Correspondent

No official correspondent registered.

US Agent Details

Christine Wang Email: Christinewang614@gmail.com Phone: (918) 9988916

Related Public Records

Same Entity

FAIRFORM MFG., 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 3012219816. Last updated year: 2026. Please use registration number 3012219816 when referencing this establishment in official correspondence.