Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003860203

FEI Number

3003860203

Entity Name

COMPOSITES BUSCH SA

City/State/Country

Porrentruy Jura, CH

Establishment Address

Chemin des Grandes Vies 54, Porrentruy Jura 2900, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Composites Busch SA (Owner Number: 10042947)

Owner / Operator Contact Address

Chemin des Grandes-Vies 54, Porrentruy, CH-JU 2900, CH

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
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2013-01-14
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2014-12-23
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2014-12-23
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-14
JEC	Component, Traction, Invasive	Orthopedic	Class 2	888.3040	2013-01-14
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2013-01-14
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-14

Official Correspondent

Nicolas Bernet

US Agent Details

Todd Garcia Email: todd.garcia@buschusa.com Phone: (484) 5668233

Related Public Records

Same Entity

Composites Busch SA

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K020905	Biomet Orthopedics, Inc.	NBX - NON-BRIDGING EXTERNAL FIXATOR	2002-04-15
K063832	Synthes (Usa)	SYNTHES (USA) ELBOW HINGE FIXATOR	2007-03-07
K030390	Synthes (Usa)	SYNTHES LARGE COMBINATION CLAMP AND DYNAMIZATION CLIP - MR SAFE	2003-04-01
K033476	Howmedica Osteonics Corp.	MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM	2004-01-20

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3015542154	Zimmer Biomet Korea Ltd.	Seoul, KR
1000517406	Paragon Medical Inc.	Smithfield, UT, US
2029275	Sterigenics U.S., LLC	Corona, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003860203. Last updated year: 2026. Please use registration number 3003860203 when referencing this establishment in official correspondence.