MASTERmatic LUX M20 L

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name: MASTERmatic LUX M20 L FDA UDI
Generic Name: Dental surgical power tool motor, electric FDA UDI
Device Name: This is a medical device. FDA UDI
Model / Reference: 1.009.3620 FDA UDI
Description: This is a medical device. FDA UDI

Identifiers

Catalog Number: M20 L FDA UDI
Primary DI / UDI-DI: EKAV100936200 FDA UDI
510(k) Number: K143465 FDA UDI
FDA Product Code: EFA FDA UDI
GMDN Term: Dental surgical power tool motor, electric 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, electric

MASTERmatic LUX M20 L by KaVo Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K143465 also covers:

A-dec — A-Dec, Inc.
A-dec — A-Dec, Inc.
A-dec — A-Dec, Inc.
A-dec — A-Dec, Inc.
MASTERmatic LUX M05 L — KaVo Dental GmbH
MASTERmatic LUX M07 L — KaVo Dental GmbH
MASTERmatic LUX M10 L — KaVo Dental GmbH
MASTERmatic LUX M25 L — KaVo Dental GmbH
MASTERmatic LUX M29 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 babb3f5d-bbe8-4691-b227-91d5ffd519d2 37 fields · synced Jun 8, 2026