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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 FDA UDI
Device Name
Cavitron® a-dec® Built-In Ultrasonic Scaler Model G90 (66 GRY). Also contains: Steri-Mate® Handpiece with Swivel cable, Ultrasonic insert, and Installation kit. FDA UDI
Model / Reference
8135001 FDA UDI
Description
Cavitron® a-dec® Built-In Ultrasonic Scaler Model G90 (66 GRY). Also contains: Steri-Mate® Handpiece with Swivel cable, Ultrasonic insert, and Installation kit. FDA UDI

Identifiers

Primary DI / UDI-DI
D00381350011 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ultrasonic dental scaling/debridement system

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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ec0f486-4d08-4f4a-be08-781e76432d20 35 fields · synced Jun 8, 2026