gudid Primary ID: DL100L

DL100 Lens (UDI DL100L)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DL100 Lens (Model/Catalog Number: DL100L) 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: DL100L
Product Code / EMDN: KYT
Device Name: 10x lens for DL100 series
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 DL100 Lens?

The registered manufacturer of record for DL100 Lens is DermLite LLC.

What is the Primary UDI-DI identifier for DL100 Lens?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DL100L.

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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