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G5 All-Purpose Desensitizer

FDA UDI

Class II (US FDA UDI)

by Clinician's Choice Dental Products, Inc.

Identity

Trade Name
G5 All-Purpose Desensitizer FDA UDI
Generic Name
Dental coating, tooth-desensitizing, professional FDA UDI
Device Name
Dental coating, tooth-desensitizing, professional FDA UDI
Model / Reference
226105 FDA UDI
Description
Dental coating, tooth-desensitizing, professional FDA UDI

Identifiers

Catalog Number
226105 FDA UDI
Primary DI / UDI-DI
07540172019125 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental coating, tooth-desensitizing, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

No

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
Total Volume — 5 Milliliter FDA UDI

Category: Dental coating, tooth-desensitizing, professional

G5 All-Purpose Desensitizer by Clinician's Choice Dental Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d66b7472-dcfd-44a1-9912-2c3799e10f5e 37 fields · synced Jun 8, 2026