gudid Primary ID: Black

FAQ Dual LED Panel (UDI Black)

Manufactured by Foreo AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FAQ Dual LED Panel (Model/Catalog Number: Black) is a medical device manufactured by Foreo AB. This product is indexed under FDA Product Code / Category Classification OHS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Black
Product Code / EMDN: OHS
Device Name: FAQ LED Panels are over-the-counter (OTC) devices intended for the treatment of wrinkles with red+ infrared light and yellow + infrared light, and the treatment of mild to moderate acne with blue+infrared light.
Database Sync Date: 2026-08-09 09:16:07

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 FAQ Dual LED Panel?

The registered manufacturer of record for FAQ Dual LED Panel is Foreo AB.

What is the Primary UDI-DI identifier for FAQ Dual LED Panel?

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

What classification code is assigned to this device?

This device is registered under product classification code OHS.

Similar Classification Devices (OHS)

Other Devices by Foreo AB

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