gudid Primary ID: Fuchsia

ESPADA 2 (UDI Fuchsia)

Manufactured by Foreo AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ESPADA 2 (Model/Catalog Number: Fuchsia) is a medical device manufactured by Foreo AB. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Fuchsia
Product Code / EMDN: OLP
Device Name: The ESPADA 2 Acne-Clearing Blue Light Pen is intended for use as an at-home device for the treatment of mild to moderate inflammatory acne.
Database Sync Date: 2026-08-09 09:48:57

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 ESPADA 2?

The registered manufacturer of record for ESPADA 2 is Foreo AB.

What is the Primary UDI-DI identifier for ESPADA 2?

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

What classification code is assigned to this device?

This device is registered under product classification code OLP.

Similar Classification Devices (OLP)

Other Devices by Foreo AB

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