gudid
Primary ID: B
FUSION Silane (UDI B)
Manufactured by Taub Products
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FUSION Silane - Primary ID B
Device Regulatory Overview
The FUSION Silane (Model/Catalog Number: B) is a medical device manufactured by Taub Products. This product is indexed under FDA Product Code / Category Classification EBO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B
- Product Code / EMDN
- EBO
- Device Name
- A two-part silane system creating a stronger chemical bond to feldspathic porcelain, all ceramic restorations, and recommended for best adhesion to veneers, crowns and other ceramic restorations.Also use it for easy chair-side repairs to: porcelain-gold restorations, porcelain jackets, porcelain denture teeth, popped-out porcelain veneers or facings. Eliminates costly laboratory remakes. This non-toxic, non-irritating formula can be used in or out of the mouth.
- Database Sync Date
- 2026-08-09 09:03:37
Full Regulatory Attributes
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{
"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 FUSION Silane?
The registered manufacturer of record for FUSION Silane is Taub Products.
What is the Primary UDI-DI identifier for FUSION Silane?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B.
What classification code is assigned to this device?
This device is registered under product classification code EBO.
Similar Classification Devices (EBO)
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