gudid Primary ID: VM80-1459

Avalign (UDI VM80-1459)

Manufactured by Avalign Technologies, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Avalign (Model/Catalog Number: VM80-1459) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification FZX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VM80-1459
Product Code / EMDN: FZX
Device Name: Kirschner Bow, Extra Long,
Database Sync Date: 2026-08-09 09:02:38

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Avalign?

The registered manufacturer of record for Avalign is Avalign Technologies, Inc..

What is the Primary UDI-DI identifier for Avalign?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VM80-1459.

What classification code is assigned to this device?

This device is registered under product classification code FZX.

Similar Classification Devices (FZX)

Other Devices by Avalign Technologies, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint