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Kwik

FDA UDI

Class II (US FDA UDI)

by Cosmedent, Inc.

Identity

Trade Name
Kwik FDA UDI
Generic Name
Dental impression material adhesive FDA UDI
Model / Reference
7031TA FDA UDI

Identifiers

Catalog Number
7031TA FDA UDI
Primary DI / UDI-DI
D7797031TA0 FDA UDI
510(k) Number
K992001 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Dental impression material adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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: Dental impression material adhesive

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

Similar devices

Also classified as Dental impression material adhesive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cosmedent, Inc.

Sources (1)

  • FDA UDI abbd43ea-fb22-4f4e-b51a-284ffb3b9777 34 fields · synced May 30, 2026