TRINITY ORTHOPEDICS, LLC

FDA Device Registration & Listing · San Diego, CA, US · Registration 3006700424

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
3006700424
FEI Number
3006700424
Entity Name
TRINITY ORTHOPEDICS, LLC
City/State/Country
San Diego, CA, US
Establishment Address
8817 Production Ave., San Diego, CA 92121, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Trinity Orthopedics, LLC (Owner Number: 10026211)
Owner / Operator Contact Address
8817 Production Ave., San Diego, CA 92121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Power Trocar Corex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTW Bit, Drill Orthopedic Class 1 888.4540 2019-12-31
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2008-06-19

Official Correspondent

James Marino

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Trinity Orthopedics, LLC
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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006700424. Last updated year: 2026. Please use registration number 3006700424 when referencing this establishment in official correspondence.
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