gudid
Primary ID: Microlux 2
AdDent (UDI Microlux 2)
Manufactured by ADDENT, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AdDent - Primary ID Microlux 2
Device Regulatory Overview
The AdDent (Model/Catalog Number: Microlux 2) is a medical device manufactured by ADDENT, INC.. This product is indexed under FDA Product Code / Category Classification NTK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Microlux 2
- Product Code / EMDN
- NTK
- Device Name
- The Microlux 2 Transilluminator is used for detecting Anterior and Posterior Caries. It also helps to visualize crown fractures, root canal orifice, and root fractures. Microlux 2 applications include an accessory for Proximal Caries detection, and Oral Cancer Screening.
- Database Sync Date
- 2026-08-09 09:03:36
Full Regulatory Attributes
🔒 Token Gated
{
"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 AdDent?
The registered manufacturer of record for AdDent is ADDENT, INC..
What is the Primary UDI-DI identifier for AdDent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Microlux 2.
What classification code is assigned to this device?
This device is registered under product classification code NTK.
Similar Classification Devices (NTK)
Other Devices by ADDENT, INC.
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