MASTERtorque Mini Kids Edition (en)

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name: MASTERtorque Mini Kids Edition (en) FDA UDI
Generic Name: Dental power tool system handpiece, pneumatic FDA UDI
Device Name: This is a medical device. FDA UDI
Model / Reference: 1.011.2330 FDA UDI
Description: This is a medical device. FDA UDI

Identifiers

Catalog Number: Kids-Edition en FDA UDI
Primary DI / UDI-DI: EKAV101123300 FDA UDI
510(k) Number: K130560 FDA UDI
FDA Product Code: EFB FDA UDI
GMDN Term: Dental power tool system handpiece, pneumatic FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool system handpiece, pneumatic

MASTERtorque Mini Kids Edition (en) by KaVo Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool system handpiece, pneumatic.

MK-dent Germany® — MK-Dent GmbH · Class I
AG Neovo — ASSOCIATED INDUSTRIES CHINA, INC. · Class I
MicroP Dental — Microp Technology (Taiwan), Inc. · Class I
AG Neovo — ASSOCIATED INDUSTRIES CHINA, INC. · Class I
SurgiPro — HENRY SCHEIN, INC. · Class I
Henry Schein — HENRY SCHEIN, INC. · Class I
PROPHY SPORT — HANDPIECE PARTS & REPAIRS, INC. · Class I
MK-dent Germany® — MK-Dent GmbH · Class I

Cleared under the same submission

K130560 also covers:

A-dec — A-Dec, Inc.
A-dec — A-Dec, Inc.
MASTERtorque LUX M8900 L — KaVo Dental GmbH
MASTERtorque Mini LUX M4500 L — KaVo Dental GmbH

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: KaVo Dental GmbH

Sources (1)

FDA UDI 37088b72-d9e0-4665-8e67-bd40819c0501 37 fields · synced Jun 1, 2026