MEDULOC

FDA Device Registration & Listing · Del Mar, CA, US · Registration 3042903229

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
3042903229
FEI Number
3042903229
Entity Name
MEDULOC
City/State/Country
Del Mar, CA, US
Establishment Address
2010 Jimmy Durante Blvd Ste 200, Del Mar, CA 92014, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Meduloc (Owner Number: 10094686)
Owner / Operator Contact Address
2010 Jimmy Durante Blvd, Suite 200, Del Mar, CA 92014, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Meduloc Intramedullary Fracture Fixation (IFF) System Meduloc Intramedullary Fracture Fixation (IFF) System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2026-01-12
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2026-01-12

Official Correspondent

Benjamin Arnold

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Meduloc
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-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042903229. Last updated year: 2026. Please use registration number 3042903229 when referencing this establishment in official correspondence.
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