AMD DISTRIBUTION SAS

FDA Device Registration & Listing · Amancy Haute-Savoie, FR · Registration 3010304009

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
3010304009
FEI Number
3010304009
Entity Name
AMD DISTRIBUTION SAS
City/State/Country
Amancy Haute-Savoie, FR
Establishment Address
579, rue de Pierre Longue, ZAE Pierre Longue II, Amancy Haute-Savoie F-74800, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AMD Distribution SAS (Owner Number: 10043179)
Owner / Operator Contact Address
579, rue de Pierre Longue, ZAE Pierre Longue II, Amancy, FR-74 F-74800, FR
Initial Importer Flag
N
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
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2013-01-29

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

AMD Distribution SAS
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-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
Z-0013-2011 Depuy Orthopaedics, Inc. 1
Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number Establishment Name Location
3018033084 NEXT GENERATION TOOLING INC Akron, OH, US
3038207124 NATIVE ORTHOPAEDICS Providence, RI, US
3027516563 STAR SPORTS MEDICINE CO., LTD. Beijing, CN
3021574846 3D LOGICS LLC Hillsboro, OR, US
3030089866 ORTOLOG MEDIKAL SANAYI VE TICARET A.S. Yenimahalle Ankara, TR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010304009. Last updated year: 2026. Please use registration number 3010304009 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.