Glu/Sense

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name: Glu/Sense FDA UDI
Generic Name: Dental cavity varnish FDA UDI
Device Name: Glu/Sense 1ml desensitizer gel syringe FDA UDI
Model / Reference: 310122 FDA UDI
Description: Glu/Sense 1ml desensitizer gel syringe FDA UDI

Identifiers

Primary DI / UDI-DI: 00817051020747 FDA UDI
510(k) Number: K955279 FDA UDI
FDA Product Code: LBH FDA UDI
GMDN Term: Dental cavity varnish FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3260 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental cavity varnish

Glu/Sense by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Centrix, Inc.

Sources (1)

FDA UDI a70087ee-450d-4572-b057-9fda2f1b9bc3 34 fields · synced May 31, 2026