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Dentin Desensitizer

FDA UDI

Class II (US FDA UDI)

by Pulpdent Corporation

Identity

Trade Name
DENTIN DESENSITIZER FDA UDI
Generic Name
Dental tooth-cleaning solution FDA UDI
Device Name
CONTAINS GLUTARALDEHYDE, FLUORIDE AND WATER 12 mL bottle FDA UDI
Model / Reference
DES FDA UDI
Description
CONTAINS GLUTARALDEHYDE, FLUORIDE AND WATER 12 mL bottle FDA UDI

Identifiers

Primary DI / UDI-DI
D701DES2 FDA UDI
510(k) Number
K963652 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental tooth-cleaning solution 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

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 tooth-cleaning solution

Dentin Desensitizer by Pulpdent Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental tooth-cleaning solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bdde392-19fd-4c50-a0ec-46c35dd8b56d 34 fields · synced Jun 9, 2026