gudid
Primary ID: 1
Reline-it (UDI 1)
Manufactured by Doc Brands, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reline-it - Primary ID 1
Device Regulatory Overview
The Reline-it (Model/Catalog Number: 1) is a medical device manufactured by Doc Brands, Inc.. This product is indexed under FDA Product Code / Category Classification EBP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- EBP
- Device Name
- The device is a temporary OTC soft, clear denture reliner consisting of 2 parts (1) a monomer liquid and (2) a polymer powder which are mixed together prior to application. This results in a plastic resin paste which is then applied to the denture plate and set in the mouth to cure for a short period of time. Once setting is complete, the excess soft material is able to be trimmed by an enclosed spatula. The application is completely reversible by soaking the denture plate overnight in an over the counter solution of hydrogen peroxide and then removing it by hand.
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Reline-it?
The registered manufacturer of record for Reline-it is Doc Brands, Inc..
What is the Primary UDI-DI identifier for Reline-it?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code EBP.
Similar Classification Devices (EBP)
Other Devices by Doc Brands, Inc.
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