IonoStar Molar (UDI 2524)

Manufactured by VOCO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The IonoStar Molar (Model/Catalog Number: 2524) is a medical device manufactured by VOCO GmbH. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2524
Product Code / EMDN: EMA
Device Name: Glass ionomer restorative material.
Database Sync Date: 2026-08-09 09:07:36

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 IonoStar Molar?

The registered manufacturer of record for IonoStar Molar is VOCO GmbH.

What is the Primary UDI-DI identifier for IonoStar Molar?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2524.

What classification code is assigned to this device?

This device is registered under product classification code EMA.

Similar Classification Devices (EMA)

Other Devices by VOCO GmbH

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