FDA UDI In Commercial Distribution 🇺🇸 United States

TRUELOK SYSTEM

DI: 18059015375923 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
TRUELOK SYSTEM
Primary DI
18059015375923
Version / Model
1
Catalog Number
50-2507
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-03
Public Version
3
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
55a2d70b-bc2a-4cc9-a754-10c8503f2e83

Device Description

TRUELOK ELEVATE TEMPLATE INSERTS

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 18059015375923

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242861 000