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Tempo Powder

FDA UDI

Class II (US FDA UDI)

by Lang Dental Manufacturing Company, Inc.

Identity

Trade Name
TEMPO POWDER FDA UDI
Generic Name
Denture reliner, soft, professional FDA UDI
Device Name
CUSHION TREATMENT DENTURE REPAIR RELINE ACRYLIC RESIN POWDER FDA UDI
Model / Reference
45.4 KG CLEAR GEL FDA UDI
Description
CUSHION TREATMENT DENTURE REPAIR RELINE ACRYLIC RESIN POWDER FDA UDI

Identifiers

Catalog Number
1080CLR FDA UDI
Primary DI / UDI-DI
D6501080CLR0 FDA UDI
510(k) Number
K081514 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, soft, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

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: Denture reliner, soft, professional

Tempo Powder by Lang Dental Manufacturing Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture reliner, soft, professional.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae514841-1eb0-49da-b7f4-959db037c136 35 fields · synced May 30, 2026