Not currently registered with FDA under this name

Scorpion

Deerfield, IL, United States. Named as applicant on 1 dental 510(k) clearance between 2006 and 2006. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12006–2006
Markets registered in: 529 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2000–2026

Registered in 5 markets

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

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Scorpion	1 clearances	2006–2006	Below
European Union	EUDAMED	Registration holder	SCORPION	23	—	Pure Global AI
Canada	Health Canada	Registration holder	SCORPION	3	2004–2015	Pure Global AI
South Korea	MFDS	Manufacturer	SCORPIONScorpion	2	2010–2020	Pure Global AI
Australia	TGA	Manufacturer	Scorpion	1	2017–2017	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 Scorpion as the applicant.

Decided	510(k)	Device	Device type
14 Jul 2006	K053578	SCORPION ULTRASONIC SCALING INSERTS	ELC Ultrasonic Scaler

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.