GUDIDData
gudid Primary ID: 316

Denture, splint (UDI 316)

Manufactured by Modern Dental Laboratory (DG) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Denture, splint - Primary ID 316

Device Regulatory Overview

The Denture, splint (Model/Catalog Number: 316) is a medical device manufactured by Modern Dental Laboratory (DG) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NSK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
316
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Denture, splint?

The registered manufacturer of record for Denture, splint is Modern Dental Laboratory (DG) Co., Ltd..

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 316.

What classification code is assigned to this device?

This device is registered under product classification code NSK.

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