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Integra

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Integra FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
EcoNomy Kit - Dust Free Dental Alginate Impression Material FDA UDI
Model / Reference
26757 FDA UDI
Description
EcoNomy Kit - Dust Free Dental Alginate Impression Material FDA UDI

Identifiers

Primary DI / UDI-DI
10841396111799 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material 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

Yes

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
Weight — 5.44 Kilogram FDA UDI

Category: Silicone dental impression material

Integra by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 519f2ef2-571b-49cf-8308-684b8cc1f4f4 36 fields · synced Jun 6, 2026