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Contour

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Contour FDA UDI
Generic Name
Dental amalgam alloy FDA UDI
Device Name
Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Double Spill FDA UDI
Model / Reference
29966 FDA UDI
Description
Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Double Spill FDA UDI

Identifiers

Primary DI / UDI-DI
10841396117647 FDA UDI
510(k) Number
K820181 FDA UDI
FDA Product Code
EJJ FDA UDI
GMDN Term
Dental amalgam alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3070 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: Dental amalgam alloy

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

Similar devices

Also classified as Dental amalgam alloy.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI d13846c4-ed6d-4406-963e-53380c449344 36 fields · synced Jun 8, 2026