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KAVO DENTAL MANUFACTURING INC.

USA · Sumas

✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada — 4 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

20listed device types

Class I 13Class II 7Class III 0

plus 33 registration records and 2 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

8registered devices

Class II 8

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

5registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

14active device licences

Class II 10Class III 4

28 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States33 registration records, 2 510(k), 0 PMA, 5 excluded

Brazil8 confirmed, 0 excluded

Saudi Arabia5 confirmed, 0 excluded

Canada14 confirmed, 4 excluded

Manufacturer names merged into this page: KAVO DENTAL GMBH · KAVO DENTAL MANUFACTURING INC. · KaVo Dental GmbH

FDA 510(k) clearances by year

12006 · K060080

12021 · K213139

FDA listed device types

showing 8 of 20

Unit, Syringe, Air And/Or Water 1Controller, Foot, Handpiece And Cord 1Handpiece, Air-Powered, Dental 1Handpiece, Contra- And Right-Angle Attachment, Dental 1Unit, Operative Dental 1Handpiece, Direct Drive, Ac-Powered 1Remover, Crown 1Light, Operating, Dental 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K213139	SURGmatic S15 L Pro	2021-12-21
US	K060080	DIAGNODENT 2190 WITH PERIODONTAL PROBE	2006-02-08
BR	81504799143	Instrumento de Mão Odontológica de Baixa Rotação	Class II
BR	81504799144	Micro Motor Odontológico	Class II
BR	81504799145	Instrumento de Mão Odontológicas de Alta Rotação	Class II
SA	ME0000000676SFDAA00096	KaVoLUX 540 LED	—
SA	ME0000001366SFDAA00001	KaVo Spray 2112	—
CA	4475	DIAGNODENT LASER	Class II
CA	6817	KAVO KEY LASER	Class III
CA	16627	KAVO INTRASURG	Class II

KAVO DENTAL MANUFACTURING INC.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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