iTero Element 2 Plus upgrade mobile configuration (UDI 211372)
Manufactured by Align Technology, Inc.
Device Regulatory Overview
The iTero Element 2 Plus upgrade mobile configuration (Model/Catalog Number: 211372) is a medical device manufactured by Align Technology, Inc.. This product is indexed under FDA Product Code / Category Classification NOF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 211372
- Product Code / EMDN
- NOF
- Device Name
- Scanner, mobile configuration
- Database Sync Date
- 2026-08-09 09:40:14
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of iTero Element 2 Plus upgrade mobile configuration?
The registered manufacturer of record for iTero Element 2 Plus upgrade mobile configuration is Align Technology, Inc..
What is the Primary UDI-DI identifier for iTero Element 2 Plus upgrade mobile configuration?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 211372.
What classification code is assigned to this device?
This device is registered under product classification code NOF.
Similar Classification Devices (NOF)
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