VELCO TOOL & DIE, INC.

FDA Device Registration & Listing · LAKE FOREST, CA, US · Registration 2029315

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
2029315
FEI Number
1000306508
Entity Name
VELCO TOOL & DIE, INC.
City/State/Country
LAKE FOREST, CA, US
Establishment Address
20431 BARENTS SEA CIRCLE, LAKE FOREST, CA 92630, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Velco Tool & Die, Inc. (Owner Number: 9010062)
Owner / Operator Contact Address
26021 Commercentre Drive, --, Lake Forest, CA 92630, US
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 2007-12-27

Official Correspondent

Christy Pennino

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Velco Tool & Die, Inc.
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 2029315. Last updated year: 2026. Please use registration number 2029315 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.