Not currently registered with FDA under this name

Westport Medical, Inc.

Salem, OR, 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: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Westport Medical, Inc. as the applicant.

Decided	510(k)	Device	Device type
17 Oct 2006	K063007	POWERTOME PERIOTOME	EKX Ac-Powered Direct Drive 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.