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Cavitron®

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
Cavitron® FDA UDI
Generic Name
Ultrasonic dental scaling/debridement system handpiece tip, periodontal FDA UDI
Device Name
Slimline® Ultrasonic Insert 25K SLI®-10L FDA UDI
Model / Reference
79292 FDA UDI
Description
Slimline® Ultrasonic Insert 25K SLI®-10L FDA UDI

Identifiers

Primary DI / UDI-DI
D003792921 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system handpiece tip, periodontal 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ultrasonic dental scaling/debridement system handpiece tip, periodontal

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

Similar devices

Also classified as Ultrasonic dental scaling/debridement system handpiece tip, periodontal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply Professional

Sources (1)

  • FDA UDI d50ad9dc-fc3c-43af-9667-af4c20e9c611 34 fields · synced Jun 8, 2026