Not currently registered with FDA under this name

Dong IL Technology , Ltd.

Hwaseong-Si, Gyeonggi-Do, South Korea. Named as applicant on 2 dental 510(k) clearances between 2011 and 2015. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22011–2015
Markets registered in: 23 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Dong IL Technology , Ltd. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: South KoreaOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Dong IL Technology , Ltd.	2 clearances	2011–2015	Below
Taiwan	TFDA	Manufacturer	DONG IL TECHNOLOGY LTD.	3	2012–2017	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 Dong IL Technology , Ltd. as the applicant.

Decided	510(k)	Device	Device type
2 Jun 2015	K150076	Sonic Surgeon 310L, Sonic Surgeon 600L and Sonic Surgeon 800L	DZI Powered Bone Drill
16 Dec 2011	K110881	ULTRASONIC SURGICAL UNIT	DZI Powered Bone Drill

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.