Neoloy (UDI N Extra Hard)

Manufactured by Dentsply International Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Neoloy (Model/Catalog Number: N Extra Hard) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EJH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N Extra Hard
Product Code / EMDN: EJH
Device Name
Database Sync Date: 2026-08-09 09:02:03

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 Neoloy?

The registered manufacturer of record for Neoloy is Dentsply International Inc..

What is the Primary UDI-DI identifier for Neoloy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N Extra Hard.

What classification code is assigned to this device?

This device is registered under product classification code EJH.

Similar Classification Devices (EJH)

Other Devices by Dentsply International Inc.

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