GL SINGLE THICKNESS WAFER (25) (UDI 260-031)
Manufactured by Great Lakes Dental Technologies, Ltd.
Device Regulatory Overview
The GL SINGLE THICKNESS WAFER (25) (Model/Catalog Number: 260-031) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification EGD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 260-031
- Product Code / EMDN
- EGD
- Device Name
- GL SINGLE THICKNESS WAFER (25)
- Database Sync Date
- 2026-08-09 09:14:54
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 GL SINGLE THICKNESS WAFER (25)?
The registered manufacturer of record for GL SINGLE THICKNESS WAFER (25) is Great Lakes Dental Technologies, Ltd..
What is the Primary UDI-DI identifier for GL SINGLE THICKNESS WAFER (25)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 260-031.
What classification code is assigned to this device?
This device is registered under product classification code EGD.
Similar Classification Devices (EGD)
Other Devices by Great Lakes Dental Technologies, Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint