Dental Device Guide
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Not currently registered with FDA under this name

Smh Biomaterial AG

Denton, TX, United States. Named as applicant on 1 dental 510(k) clearance between 2007 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12007–2007
Markets registered in
1United States
Establishments
0—
2007: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Smh Biomaterial AG as the applicant.

Decided510(k)DeviceDevice type
13 Dec 2007K073040SMH FLEX SEBI Rebasing Repairing Relining Denture Resin

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.