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Prosthetic Silicone Materials

FDA UDI

Class I (US FDA UDI)

by Technovent Limited

Identity

Trade Name
Prosthetic Silicone Materials FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Silicone polymer-based additives designed to thicken uncured prosthetic silicones. FDA UDI
Model / Reference
AntiSlump Agent – 20g FDA UDI
Description
Silicone polymer-based additives designed to thicken uncured prosthetic silicones. FDA UDI

Identifiers

Catalog Number
M514(20) FDA UDI
Primary DI / UDI-DI
05060483012124 FDA UDI
FDA Product Code
GBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, resin

Prosthetic Silicone Materials by Technovent Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technovent Limited

Sources (1)

  • FDA UDI c103d3ac-3542-44da-8aa5-85ad30f57a49 35 fields · synced May 30, 2026