Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009561590

FEI Number

3009561590

Entity Name

THE CHINA FACTORY COMPANY LIMITED

City/State/Country

Dongguan City Guangdong, CN

Establishment Address

78 Longhuan Rd, Dongguan City Guangdong 523710, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

The China Factory Company Limited (Owner Number: 10040303)

Owner / Operator Contact Address

78 Longhuan Rd, Dongguan City, CN-GD 523710, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cryo Pack The Boxer Splint Knee Pneumatic Cryo Compression Device Sleeper Brace Shoulder Pneumatic Cryo Compression Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2018-04-02
ILH	Splint, Hand, And Components	Physical Medicine	Class 1	890.3475	2012-03-29
IQI	Orthosis, Limb Brace	Physical Medicine	Class 1	890.3475	2013-06-23

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

The China Factory Company 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 3009561590. Last updated year: 2026. Please use registration number 3009561590 when referencing this establishment in official correspondence.