Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004941235

FEI Number

3004941235

Entity Name

KING LIFE TECHNOLOGY CO.,LTD.

City/State/Country

Neihu Taipei, TW

Establishment Address

No.232, Shin Hu 2nd Rd, Neihu Taipei 114, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

KING LIFE TECHNOLOGY CO.,LTD. (Owner Number: 10032483)

Owner / Operator Contact Address

No.232, Shin Hu 2nd Rd, Neihu, TW-TPE 114, TW

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
KQW	Goniometer, Nonpowered	Orthopedic	Class 1	888.1520	2010-05-18

Official Correspondent

No official correspondent registered.

US Agent Details

Kevin Walls Business: Regulatory Insight, Inc. Email: kevin@reginsight.com Phone: (720) 9625412

Related Public Records

Same Entity

KING LIFE TECHNOLOGY CO.,LTD.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
1720747	SONTEC INSTRUMENTS, INC.	CENTENNIAL, CO, US
3004526603	RICHARDSON PRODUCTS, INC.	FRANKFORT, IL, US
8010547	STORK INSTRUMENTE GMBH	Emmingen-Liptingen Baden-Wurttemberg, DE
2027754	OSTEOMED	ADDISON, TX, US
3007366790	Smith & Nephew, Inc.	Memphis, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004941235. Last updated year: 2026. Please use registration number 3004941235 when referencing this establishment in official correspondence.