GUDIDData
gudid Primary ID: 404

Denture, Restoration (UDI 404)

Manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Denture, Restoration - Primary ID 404

Device Regulatory Overview

The Denture, Restoration (Model/Catalog Number: 404) is a medical device manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED. This product is indexed under FDA Product Code / Category Classification NSK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
404
Product Code / EMDN
NSK
Device Name
Database Sync Date
2026-08-09 09:06:41

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 Denture, Restoration?

The registered manufacturer of record for Denture, Restoration is ACESO DENTAL LABORATORY COMPANY LIMITED.

What is the Primary UDI-DI identifier for Denture, Restoration?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 404.

What classification code is assigned to this device?

This device is registered under product classification code NSK.

Programmatic Export

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

JSON API Endpoint