Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009560848

FEI Number

3009560848

Entity Name

SPECIAL HEADWAY(HK) LIMITED

City/State/Country

kowloon hong kong, HK

Establishment Address

flat Q 9/F, 38 yuet wah street, Kwun tong kowloon, kowloon hong kong 999077, HK

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Special Headway Limited (Owner Number: 10040299)

Owner / Operator Contact Address

flat Q 9/F, 38 yuet wah street, Kwun tong kowloon, kowloon hong kong, HK-NOTA 999077, 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
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2012-11-30
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2012-03-29

Official Correspondent

david lehrer

US Agent Details

david lehrer Email: fdadave@gmail.com Phone: (718) 4514444

Related Public Records

Same Entity

Special Headway 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 3009560848. Last updated year: 2026. Please use registration number 3009560848 when referencing this establishment in official correspondence.