7LS (UDI FA7-1450J)

Manufactured by FKA DISTRIBUTING CO., LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 7LS (Model/Catalog Number: FA7-1450J) is a medical device manufactured by FKA DISTRIBUTING CO., LLC. This product is indexed under FDA Product Code / Category Classification OHS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FA7-1450J
Product Code / EMDN: OHS
Device Name: ReNew Light Therapy
Database Sync Date: 2026-08-09 09:00:32

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 7LS?

The registered manufacturer of record for 7LS is FKA DISTRIBUTING CO., LLC.

What is the Primary UDI-DI identifier for 7LS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FA7-1450J.

What classification code is assigned to this device?

This device is registered under product classification code OHS.

Similar Classification Devices (OHS)

Other Devices by FKA DISTRIBUTING CO., LLC

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