Not currently registered with FDA under this name

Alexotek Co.

Eugene, OR, United States. Named as applicant on 4 dental 510(k) clearances between 1984 and 1988. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 41984–1988
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Alexotek Co. as the applicant.

Decided	510(k)	Device	Device type
1 Jun 1988	K881789	MINILINE BRACKET	EJF Orthodontic Metal Bracket
5 Apr 1984	K834446	ALEXOTEK LINGUAL TUBES	DZD Orthodontic Tube
28 Feb 1984	K834392	LABIAL CUSPID TUBE	DZD Orthodontic Tube
3 Feb 1984	K834272	ALEXOLOK BRACKET	EJF Orthodontic Metal Bracket

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.