Stoneglass Industries (UDI SGI105)
Manufactured by STONEGLASS DENTAL LABORATORY PTY LTD
Device Regulatory Overview
The Stoneglass Industries (Model/Catalog Number: SGI105) is a medical device manufactured by STONEGLASS DENTAL LABORATORY PTY LTD. This product is indexed under FDA Product Code / Category Classification NSL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SGI105
- Product Code / EMDN
- NSL
- Device Name
- Temporary Prosthesis Assembled with Temporary Cylinders
- Database Sync Date
- 2026-08-09 09:01:55
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 Stoneglass Industries?
The registered manufacturer of record for Stoneglass Industries is STONEGLASS DENTAL LABORATORY PTY LTD.
What is the Primary UDI-DI identifier for Stoneglass Industries?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SGI105.
What classification code is assigned to this device?
This device is registered under product classification code NSL.
Similar Classification Devices (NSL)
Other Devices by STONEGLASS DENTAL LABORATORY PTY LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint