← Back to catalogue

SimpliShade

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
SimpliShade FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Nanohybrid Universal Composite Restorative, Unidose, Shade Medium FDA UDI
Model / Reference
37007 FDA UDI
Description
Nanohybrid Universal Composite Restorative, Unidose, Shade Medium FDA UDI

Identifiers

Primary DI / UDI-DI
00841396198953 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

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

Dimensions & Sizes

Size
Weight — 5 Gram FDA UDI

Category: Dental composite resin

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

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI a0ad368f-ad3a-482d-8263-bd0df6c4ad9f 36 fields · synced Jun 8, 2026