gudid Primary ID: Black

FAQ 202 (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 202 (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 202 is intended to use LED light for the treatment of wrinkles and mild to moderate acne.
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 202?

The registered manufacturer of record for FAQ 202 is Foreo AB.

What is the Primary UDI-DI identifier for FAQ 202?

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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