gudid Primary ID: SKL2

INACTIVE - Skinlite II (UDI SKL2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The INACTIVE - Skinlite II (Model/Catalog Number: SKL2) is a medical device manufactured by DermLite LLC. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1506-2023 View Full Alert →

DERMLITE DL4W, REF: DL4W, Rx Only MD, CE...

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Technical Specifications

Model Number: SKL2
Product Code / EMDN: KYT
Device Name: INACTIVE - Skinlite II
Database Sync Date: 2026-08-09 09:37:45

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 INACTIVE - Skinlite II?

The registered manufacturer of record for INACTIVE - Skinlite II is DermLite LLC.

What is the Primary UDI-DI identifier for INACTIVE - Skinlite II?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SKL2.

What classification code is assigned to this device?

This device is registered under product classification code KYT.

Similar Classification Devices (KYT)

Other Devices by DermLite LLC

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