gudid Primary ID: LYFT3

NURYSH (UDI LYFT3)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NURYSH (Model/Catalog Number: LYFT3) is a medical device manufactured by UPLEVITY LLC. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LYFT3
Product Code / EMDN: OLP
Device Name: A portable electrically-powered device intended to emit both red and blue light for the treatment of a facial skin condition (e.g., acne, hyperpigmentation) by the patient in the home. It includes integral lights with a controller/controlling interface (to pair with an off-the-shelf computer/smartphone), and may be available in a variety of forms (e.g., a face-worn light mask with controller, hand-held light unit). It is not intended for use with a photosensitizing agent. This is a single-patient, reusable device.
Database Sync Date: 2026-08-09 09:49:29

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 NURYSH?

The registered manufacturer of record for NURYSH is UPLEVITY LLC.

What is the Primary UDI-DI identifier for NURYSH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LYFT3.

What classification code is assigned to this device?

This device is registered under product classification code OLP.

Similar Classification Devices (OLP)

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