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Cavitron®

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
Cavitron® FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
Prophy-Jet® Mint Flavored Sodium Bicarbonate Prophy Powder 364g FDA UDI
Model / Reference
130002 FDA UDI
Description
Prophy-Jet® Mint Flavored Sodium Bicarbonate Prophy Powder 364g FDA UDI

Identifiers

Primary DI / UDI-DI
D0031300021 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 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: Dentifrice

Cavitron® by Dentsply Professional — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a357e40c-612d-4756-891c-e4f76347d500 35 fields · synced May 30, 2026