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OptiGuard

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
OptiGuard FDA UDI
Generic Name
Dental unfilled resin sealant/coating FDA UDI
Device Name
Light Cure Composite Surface Sealant; Kit FDA UDI
Model / Reference
26685 FDA UDI
Description
Light Cure Composite Surface Sealant; Kit FDA UDI

Identifiers

Catalog Number
26685 FDA UDI
Primary DI / UDI-DI
00841396108228 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental unfilled resin sealant/coating 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

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

Yes

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
Total Volume — 10 Milliliter FDA UDI

Category: Dental unfilled resin sealant/coating

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

Similar devices

Also classified as Dental unfilled resin sealant/coating.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 6aa24fca-ddba-450c-9b7f-c20ecea38552 37 fields · synced Jun 8, 2026