GUDIDData
gudid Primary ID: 857-VX-2125W

NT3 (UDI 857-VX-2125W)

Manufactured by AMERICAN ORTHODONTICS CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NT3 - Primary ID 857-VX-2125W

Device Regulatory Overview

The NT3 (Model/Catalog Number: 857-VX-2125W) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification DZC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
857-VX-2125W
Product Code / EMDN
DZC
Device Name
WIRE NITI VLP LG UNIV 021X025 IND 10/PK
Database Sync Date
2026-08-09 09:00:41

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 NT3?

The registered manufacturer of record for NT3 is AMERICAN ORTHODONTICS CORPORATION.

What is the Primary UDI-DI identifier for NT3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 857-VX-2125W.

What classification code is assigned to this device?

This device is registered under product classification code DZC.

Programmatic Export

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

JSON API Endpoint