GUDIDData
gudid Primary ID: 760

Roydent (UDI 760)

Manufactured by ROYDENT DENTAL PRODUCTS INC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Roydent - Primary ID 760

Device Regulatory Overview

The Roydent (Model/Catalog Number: 760) is a medical device manufactured by ROYDENT DENTAL PRODUCTS INC. This product is indexed under FDA Product Code / Category Classification LFC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
760
Product Code / EMDN
LFC
Device Name
TO DYE FOR
Database Sync Date
2026-08-09 09:05:41

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 Roydent?

The registered manufacturer of record for Roydent is ROYDENT DENTAL PRODUCTS INC.

What is the Primary UDI-DI identifier for Roydent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 760.

What classification code is assigned to this device?

This device is registered under product classification code LFC.

Programmatic Export

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

JSON API Endpoint