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CediTEC

FDA UDI

Class II (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
CediTEC FDA UDI
Generic Name
Denture reliner, hard FDA UDI
Device Name
Luting of prefabricated prosthetic teeth in denture basis, repair and extension of dental prosthesis FDA UDI
Model / Reference
6082 FDA UDI
Description
Luting of prefabricated prosthetic teeth in denture basis, repair and extension of dental prosthesis FDA UDI

Identifiers

Catalog Number
6082 FDA UDI
Primary DI / UDI-DI
E22160821 FDA UDI
510(k) Number
K220743 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, hard FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture reliner, hard

CediTEC by VOCO GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture reliner, hard.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI be53a3bf-6874-4bc6-8007-f8ce0f9c45fb 37 fields · synced May 30, 2026