GUDIDData
gudid Primary ID: 300-309

LG HICKHAM PROTRACTION *O (UDI 300-309)

Manufactured by Great Lakes Dental Technologies, Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LG HICKHAM PROTRACTION *O - Primary ID 300-309

Device Regulatory Overview

The LG HICKHAM PROTRACTION *O (Model/Catalog Number: 300-309) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification DZB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
300-309
Product Code / EMDN
DZB
Device Name
LG HICKHAM PROTRACTION *O
Database Sync Date
2026-08-09 09:14:54

Full Regulatory Attributes

🔒 Token Gated
{
    "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 LG HICKHAM PROTRACTION *O?

The registered manufacturer of record for LG HICKHAM PROTRACTION *O is Great Lakes Dental Technologies, Ltd..

What is the Primary UDI-DI identifier for LG HICKHAM PROTRACTION *O?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 300-309.

What classification code is assigned to this device?

This device is registered under product classification code DZB.

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