Not currently registered with FDA under this name

Kavo DO Brasil Industria E Comercio Ltda

Santa Catarina, Brazil. Named as applicant on 1 dental 510(k) clearance between 2015 and 2015. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12015–2015
Markets registered in: 552 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2007–2026

Registered in 5 markets

Where regulators' registries name Kavo DO Brasil Industria E Comercio Ltda as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: BrazilOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Kavo DO Brasil Industria E Comercio Ltda	1 clearances	2015–2015	Below
Colombia	INVIMA	Registration holder	KAVO DO BRASIL INDUSTRIA E COMERCIO LTDA.KAVO DO BRASIL INDUSTRIA E COMERCIO LTDA	31	—	Pure Global AI
Costa Rica	Ministerio de Salud	Manufacturer	KAVO DO BRASIL INDUSTRIA E COMERCIO LTDA	13	—	Pure Global AI
Canada	Health Canada	Registration holder	KAVO DO BRASIL INDUSTRIA E COMERCIO LTDA	6	2016–2016	Pure Global AI
South Korea	MFDS	Manufacturer	KaVo do Brasil Industria e Comercio Ltda.KaVo do Brasil Industriae Comercio Ltda.	2	2012–2012	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Kavo DO Brasil Industria E Comercio Ltda as the applicant.

Decided	510(k)	Device	Device type
4 May 2015	K141576	Maxima PRO 45L	EFB Dental Air-Powered Handpiece

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.