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Tylok® Plus Anhydrous Polycarboxylate Cement

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
Tylok® Plus Anhydrous Polycarboxylate Cement FDA UDI
Generic Name
Zinc polycarboxylate dental cement FDA UDI
Device Name
Tylok® Plus Anhydrous Polycarboxylate Cement Standard Package FDA UDI
Model / Reference
620200 FDA UDI
Description
Tylok® Plus Anhydrous Polycarboxylate Cement Standard Package FDA UDI

Identifiers

Catalog Number
620200 FDA UDI
Primary DI / UDI-DI
D0026202001 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Zinc polycarboxylate dental cement 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

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

Yes

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

Dimensions & Sizes

Size
Weight — 50 Gram FDA UDI

Category: Zinc polycarboxylate dental cement

Tylok® Plus Anhydrous Polycarboxylate Cement by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Zinc polycarboxylate dental cement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply International

Sources (1)

  • FDA UDI 73c82d29-8676-4f1f-82e7-66f424739aa3 37 fields · synced May 30, 2026