Dental Device Guide
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Not currently registered with FDA under this name

Dentamax, Inc.

Corvallis, OR, United States. Named as applicant on 2 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
21999–1999
Markets registered in
1United States
Establishments
0—
1999: 21990200020102020

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Dentamax, Inc. as the applicant.

Decided510(k)DeviceDevice type
23 Mar 1999K990448THE.R.MO.FREEEBI Rebasing Repairing Relining Denture Resin
7 Jan 1999K983558ACETAL DENTAL/PREFORMED CLASPEHP Preformed Clasp

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.