gudid Primary ID: 39-479

Dental City (UDI 39-479)

Manufactured by ICP, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Dental City (Model/Catalog Number: 39-479) is a medical device manufactured by ICP, INC.. This product is indexed under FDA Product Code / Category Classification EKQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 39-479
Product Code / EMDN: EKQ
Device Name: Hedstrom Files 25mm #70
Database Sync Date: 2026-08-09 09:14:55

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 Dental City?

The registered manufacturer of record for Dental City is ICP, INC..

What is the Primary UDI-DI identifier for Dental City?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 39-479.

What classification code is assigned to this device?

This device is registered under product classification code EKQ.

Similar Classification Devices (EKQ)

Other Devices by ICP, INC.

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