Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004715683

FEI Number

3004715683

Entity Name

Memphis Logistic Center

City/State/Country

Memphis, TN, US

Establishment Address

3955 E. Holmes Rd, Memphis, TN 38118, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

DePuy Synthes, Inc. (Owner Number: 1818910)

Owner / Operator Contact Address

700 Orthopaedic Drive, Warsaw, IN 46582, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

various broach instruments ATTUNE REVISION TIBIAL BROACH 45MM ATTUNE REVISION TIBIAL BROACH 61MM ATTUNE REVISION TIBIAL BROACH 37MM ATTUNE REVISION TIBIAL BROACH 29MM ATTUNE REVISION TIBIAL BROACH 53MM ATTUNE REVISION TIBIAL BROACH 69MM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTQ	Broach	Orthopedic	Class 1	888.4540	1993-01-04
KBO	Guillotine, Tonsil	Ear, Nose, Throat	Class 1	874.4420	1981-03-02

Official Correspondent

Matthew Mills

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DePuy Synthes, Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3009421413	GMED Healthcare BV (a Johnson & Johnson Company)	Leeds, GB
3015516266	Depuy Ireland UC	Co. Cork Munster, IE
1219655	DEPUY ORTHOPAEDICS, INC.	RAYNHAM, MA, US
3004464325	DEPUY ORTHOPAEDICS	BRIDGEWATER, MA, US
1818910	DEPUY ORTHOPAEDICS, INC.	WARSAW, IN, US

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3010388970	GUANGZHOU AQUILA PRECISE TOOLS LIMITED	Guangzhou City Guangdong, CN
3003596442	TRIGON AMERICA LLC	Aurora, IL, US
1038671	EXACTECH, INC.	GAINESVILLE, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004715683. Last updated year: 2026. Please use registration number 3004715683 when referencing this establishment in official correspondence.