Not currently registered with FDA under this name

Euroteknika

Montreal, Quebec, Canada. Named as applicant on 2 dental 510(k) clearances between 2009 and 2009. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22009–2009
Markets registered in: 2230 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2000–2026

Registered in 2 markets

Where regulators' registries name Euroteknika as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: CanadaOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Euroteknika	2 clearances	2009–2009	Below
Canada	Health Canada	Registration holder	EUROTEKNIKA	230	2009–2011	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 Euroteknika as the applicant.

Decided	510(k)	Device	Device type
23 Jul 2009	K083670	UNIVERSAL, AESTHETICA, NATEA, NATURA	DZE Root-Form Endosseous Implant
8 Jun 2009	K083669	OBI	DZE Root-Form Endosseous Implant

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.