gudid Primary ID: ASM-030

Agilon Surgical Matrix (UDI ASM-030)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Agilon Surgical Matrix (Model/Catalog Number: ASM-030) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ASM-030
Product Code / EMDN: KGN
Device Name
Database Sync Date: 2026-08-09 09:43:40

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 Agilon Surgical Matrix?

The registered manufacturer of record for Agilon Surgical Matrix is Biogennix, LLC.

What is the Primary UDI-DI identifier for Agilon Surgical Matrix?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ASM-030.

What classification code is assigned to this device?

This device is registered under product classification code KGN.

Similar Classification Devices (KGN)

Other Devices by Biogennix, LLC

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