gudid Primary ID: 20191

Invisalign IPR Sub-Assembly (UDI 20191)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Invisalign IPR Sub-Assembly (Model/Catalog Number: 20191) is a medical device manufactured by Align Technology, Inc.. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 20191
Product Code / EMDN: DZP
Device Name
Database Sync Date: 2026-08-09 09:37:40

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 Invisalign IPR Sub-Assembly?

The registered manufacturer of record for Invisalign IPR Sub-Assembly is Align Technology, Inc..

What is the Primary UDI-DI identifier for Invisalign IPR Sub-Assembly?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20191.

What classification code is assigned to this device?

This device is registered under product classification code DZP.

Similar Classification Devices (DZP)

Other Devices by Align Technology, Inc.

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