GUDIDData
gudid Primary ID: 02-00551

Targeting Guide (UDI 02-00551)

Manufactured by Treace Medical Concepts, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Targeting Guide - Primary ID 02-00551

Device Regulatory Overview

The Targeting Guide (Model/Catalog Number: 02-00551) is a medical device manufactured by Treace Medical Concepts, Inc.. This product is indexed under FDA Product Code / Category Classification FZX within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2718-2024 View Full Alert →

Nanoplasty 3D Bunion Correction System Implant, Model Number: SK57. System contains the 01-00066 1st Metatarsal Plate as a component....

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Technical Specifications

Model Number
02-00551
Product Code / EMDN
FZX
Device Name
SpeedMTP Targeting Guide 1.4mm K-Wire
Database Sync Date
2026-08-09 09:12:30

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Targeting Guide?

The registered manufacturer of record for Targeting Guide is Treace Medical Concepts, Inc..

What is the Primary UDI-DI identifier for Targeting Guide?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 02-00551.

What classification code is assigned to this device?

This device is registered under product classification code FZX.

Programmatic Export

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