gudid
Primary ID: 10-000-KY
MASTER-DENT (UDI 10-000-KY)
Manufactured by DENTONICS INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MASTER-DENT - Primary ID 10-000-KY
Device Regulatory Overview
The MASTER-DENT (Model/Catalog Number: 10-000-KY) is a medical device manufactured by DENTONICS INC. This product is indexed under FDA Product Code / Category Classification within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-000-KY
- Product Code / EMDN
- N/A
- Device Name
- Zinc Phosphate Cement, 32gm Powder, 17.5ml Liquid (Yellow)
- Database Sync Date
- 2026-08-09 09:31:30
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 MASTER-DENT?
The registered manufacturer of record for MASTER-DENT is DENTONICS INC.
What is the Primary UDI-DI identifier for MASTER-DENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-000-KY.
What classification code is assigned to this device?
This device is registered under product classification code .
Similar Classification Devices ()
Other Devices by DENTONICS INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint