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Tempro Blue

FDA UDI

Class II (US FDA UDI)

by Spident Co., Ltd.

Identity

Trade Name
Tempro Blue FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Light cured, single component, provisional filling material for temporary restorations. FDA UDI
Model / Reference
101-1501 FDA UDI
Description
Light cured, single component, provisional filling material for temporary restorations. FDA UDI

Identifiers

Catalog Number
101-1501 FDA UDI
Primary DI / UDI-DI
08809262954173 FDA UDI
510(k) Number
K100413 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Category: Dental composite resin

Tempro Blue by Spident Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

K100413 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spident Co., Ltd.

Sources (1)

  • FDA UDI 0d492446-2ede-4be4-ae99-539b9a6893de 36 fields · synced May 30, 2026