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Tempit

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Tempit FDA UDI
Generic Name
Temporary dental crown/bridge FDA UDI
Device Name
Tempit Essentials prefilled temporary filling material tips Kit FDA UDI
Model / Reference
310067 FDA UDI
Description
Tempit Essentials prefilled temporary filling material tips Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00817051020051 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Temporary dental crown/bridge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

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

Yes

FDA UDI

Category: Temporary dental crown/bridge

Tempit by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI b7982e33-b360-42cc-ab28-a74fe447d8b6 33 fields · synced May 30, 2026