Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010332206

FEI Number

3010332206

Entity Name

BRADFORD TOOL GROUP

City/State/Country

Bradford York, GB

Establishment Address

1 Tong Street, Bradford, West Yorkshire, Bradford York BD4 9PW, GB

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Bradford Tool Group (Owner Number: 10043332)

Owner / Operator Contact Address

1 Tong Street, Bradford, West Yorkshire, Bradford, GB-BRD BD4 9PW, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ARCOS 5.1MM DRILL - LONG ARCOS 3.6MM DRILL ARCOS IMPACTION HANDLE ARCOS INNER GUIDE TUBE; ARCOS OUTER GUIDE TUBE ARCOS TARGET SECURING BOLT Orthopedic Manual ARCOS TROCAR ACROS 3.5MM T-Handle Hex Drive

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2013-02-06
HWA	Impactor	Orthopedic	Class 1	888.4540	2013-02-06
IQO	Device, Prosthesis Alignment	Physical Medicine	Class 1	890.3025	2013-02-06
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2013-02-06

Official Correspondent

Helen Senior

US Agent Details

Theresa Ramirez Business: Emergo by UL Email: lst.aus.usagent@ul.com Phone: (512) 2220262

Related Public Records

Same Entity

Bradford Tool Group

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0010-2008	N/A	1	EPIK KNEE SYSTEM Angled Insert Impactor RM/LL; Part #801-03-052 Rev. A; non-sterile; knee prosthesis instrument. Distributed by Encore Medical, L.P., Austin, TX 78758.
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105

Similar Registrations

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2031917	CLASSIC WIRE CUT COMPANY, INC.	Valencia, CA, US
3003431869	HILBRO INTERNATIONAL (PVT) LIMITED	SIALKOT Punjab, PK
3023265483	PHEN'X TECHNOLOGIES	Chassieu Auvergne-Rhone-Alpes, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010332206. Last updated year: 2026. Please use registration number 3010332206 when referencing this establishment in official correspondence.