Guide

GUDID 00810111225403

Targeting Guide

Treace Medical Concepts, Inc.

Surgical drill guide, reusable

• Primary Device ID: 00810111225403
• NIH Device Record Key: d40caeec-9e94-4ebc-b3fe-0581aeace568
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide
• Version Model Number: 02-00422
• Company DUNS: 054808082
• Company Name: Treace Medical Concepts, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810111225403 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

[00810111225403]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-02
• Device Publish Date: 2026-01-23

On-Brand Devices [Guide]

• 00810111224031: MIS Guide
• 00810111224024: MIS Cup
• 00810111225403: Targeting Guide
• 00810111225397: Targeting Guide