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D/Sense

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
D/Sense FDA UDI
Generic Name
Dental cavity varnish FDA UDI
Device Name
D/Sense Crystal 1ml desensitizer gel syringe, 6 FDA UDI
Model / Reference
310106 FDA UDI
Description
D/Sense Crystal 1ml desensitizer gel syringe, 6 FDA UDI

Identifiers

Primary DI / UDI-DI
00817051021331 FDA UDI
510(k) Number
K120176 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental cavity varnish

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

Similar devices

Also classified as Dental cavity varnish.

Cleared under the same submission

K120176 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 0cb1269a-028c-4ee1-af41-c0aaa091ee88 34 fields · synced May 30, 2026