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Telio Desensitizer

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
Telio Desensitizer FDA UDI
Generic Name
Dental coating, tooth-desensitizing, professional FDA UDI
Device Name
Telio Desensitizer Refill 50x0.1g FDA UDI
Model / Reference
701960 FDA UDI
Description
Telio Desensitizer Refill 50x0.1g FDA UDI

Identifiers

Catalog Number
701960 FDA UDI
Primary DI / UDI-DI
DVIV7019601 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental coating, tooth-desensitizing, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental coating, tooth-desensitizing, professional

Telio Desensitizer by Ivoclar Vivadent Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e8774e9b-fad6-4d06-9565-6c893fd9c148 34 fields · synced May 30, 2026