Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005374248

FEI Number

3005374248

Entity Name

FOOK TIN TECHNOLOGIES LIMITED

City/State/Country

QUARRY BAY, HK

Establishment Address

4/F., EASTERN CENTRE, 1065 KINGS ROAD, QUARRY BAY --, HK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FOOK TIN TECHNOLOGIES LIMITED (Owner Number: 9078046)

Owner / Operator Contact Address

4/F., EASTERN CENTRE, 1065 KING'S ROAD, QUARRY BAY, HK-NOTA --, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Scaleman SCALEMAN PTI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MNW	Analyzer, Body Composition	Cardiovascular	Class 2	870.2770	2009-05-17
FRI	Scale, Stand-On, Patient	General Hospital	Class 1	880.2700	2005-09-28

Official Correspondent

JOHN CHAI

US Agent Details

Tuck Lee Email: Tuckster888@Yahoo.Com Phone: (212) 6612489

Related Public Records

Same Entity

FOOK TIN TECHNOLOGIES LIMITED

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K994242	Bodystat , Ltd.	BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT	2000-03-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005374248. Last updated year: 2026. Please use registration number 3005374248 when referencing this establishment in official correspondence.