Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009097552

FEI Number

3009097552

Entity Name

C-PRO DIRECT LTD

City/State/Country

Edenbridge Kent, GB

Establishment Address

7a The Industrial Estate, Enterprise Way, Edenbridge Kent TN8 6HF, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

C-Pro Direct Ltd (Owner Number: 10040405)

Owner / Operator Contact Address

7a The Industrial Estate, Enterprise Way, Edenbridge, GB-KEN TN8 6HF, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dorsi Ramp ADM External Rotation Bar ADM AFO ADM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2012-04-10
KNP	Orthosis, Corrective Shoe	Physical Medicine	Class 1	890.3475	2014-03-13

Official Correspondent

Yan Li

US Agent Details

Matthew Dobbs Business: KiddFoot INC Email: salesforce@kiddfoot.com Phone: (561) 7882639

Related Public Records

Same Entity

C-Pro Direct Ltd

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3013132310	FUKO INC.	Taichung, TW
3031209582	BLOCK THERAPY LTD	Winnipeg Manitoba, CA
3010163710	KUNSHAN CHENGYI GARMENT FACTORY	Kunshan Jiangsu, CN
3010393580	ARTIC BITES, LLC	Findlay, OH, US
3021194555	SALUTE REHAB, LTD.	Karmi'El Northern, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009097552. Last updated year: 2026. Please use registration number 3009097552 when referencing this establishment in official correspondence.