gudid Primary ID: KL

KLYO (UDI KL)

Manufactured by KLYO MEDICAL SYSTEMS INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The KLYO (Model/Catalog Number: KL) is a medical device manufactured by KLYO MEDICAL SYSTEMS INC.. This product is indexed under FDA Product Code / Category Classification FQO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: KL
Product Code / EMDN: FQO
Device Name: Mobile, electro- motorized table designed to be adjusted to support a patient during many types of surgical interventions. The table surface consists of many articulated sections that can be elevated or lowered for contouring to accommodate numerous anatomical positions to satisfy the requirements of many clinical specialties.
Database Sync Date: 2026-08-09 09:06:29

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 KLYO?

The registered manufacturer of record for KLYO is KLYO MEDICAL SYSTEMS INC..

What is the Primary UDI-DI identifier for KLYO?

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

What classification code is assigned to this device?

This device is registered under product classification code FQO.

Similar Classification Devices (FQO)

Other Devices by KLYO MEDICAL SYSTEMS INC.

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