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Tenure®

FDA UDI

Class II (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Tenure® FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
TENURE 4G BONDING SYSTEM FDA UDI
Model / Reference
TEN4000 FDA UDI
Description
TENURE 4G BONDING SYSTEM FDA UDI

Identifiers

Catalog Number
TEN4000 FDA UDI
Primary DI / UDI-DI
D813TEN40000 FDA UDI
510(k) Number
K140537 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine bonding agent/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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: Dentine bonding agent/set

Tenure® by Den-Mat Holdings, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine bonding agent/set.

Cleared under the same submission

K140537 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Den-Mat Holdings, LLC

Sources (1)

  • FDA UDI 8d4f8b6d-2555-483c-a5f9-5f7860a513b1 37 fields · synced Jun 9, 2026