Not currently registered with FDA under this name

Mitek Products

Westwood, MA, United States. Named as applicant on 3 dental 510(k) clearances between 1999 and 1999. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31999–1999
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Mitek Products as the applicant.

Decided	510(k)	Device	Device type
29 Dec 1999	K993575	RESOLVE QUICKANCHOR	DZL Intraosseous Fixation Screw
16 Dec 1999	K993327	TALON ANCHOR SNAP-PAK	DZL Intraosseous Fixation Screw
2 Nov 1999	K992623	MITEK MINI ANCHOR	DZL Intraosseous Fixation Screw

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.