NEW TOP GLOBAL CO., LTD.

FDA Device Registration & Listing · Kowloon, HK · Registration 3008247697

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008247697
FEI Number
3008247697
Entity Name
NEW TOP GLOBAL CO., LTD.
City/State/Country
Kowloon, HK
Establishment Address
Room 604, Kalok Building, 720 Nathan Road, Kowloon 000, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
New Top Global Co., Ltd. (Owner Number: 10031347)
Owner / Operator Contact Address
Room 604, Kalok Building, 720 Nathan Road, Kowloon, HK-NOTA 000, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Corrective Shoe Orthosis Heel Rest Arm Sling Knee Brace Cast Shoe Ankle Brace

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2018-11-21
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2010-01-19
ILI Sling, Arm Physical Medicine Class 1 890.3640 2010-01-19
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2010-01-19
IPG Shoe, Cast Physical Medicine Class 1 890.3025 2018-11-21
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2010-01-19

Official Correspondent

No official correspondent registered.

US Agent Details

Shu-Chen Cheng Business: ROC Chinese-European Industrial Research Society Email: ceirs.jen@msa.hinet.net Phone: (614) 5888168

Related Public Records

Same Entity

New Top Global 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 3008247697. Last updated year: 2026. Please use registration number 3008247697 when referencing this establishment in official correspondence.
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