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TempSpan

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
TempSpan FDA UDI
Generic Name
Temporary dental crown/bridge FDA UDI
Device Name
Temporary C&B Material; A3.5 FDA UDI
Model / Reference
N69AE FDA UDI
Description
Temporary C&B Material; A3.5 FDA UDI

Identifiers

Primary DI / UDI-DI
00814978022229 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Temporary dental crown/bridge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

Dimensions & Sizes

Size
Total Volume — 50 Milliliter FDA UDI

Category: Temporary dental crown/bridge

TempSpan by Kerr Corporation — 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
Kerr Corporation

Sources (1)

  • FDA UDI c3cb92a9-93df-47e0-b2cd-51b6515e8eac 36 fields · synced Jun 8, 2026