Dental Device Guide
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Not currently registered with FDA under this name

Terumo Corp.

Washington, DC, United States. Named as applicant on 1 dental 510(k) clearance between 2004 and 2004. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12004–2004
Markets registered in
1United States
Establishments
0—
2004: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Terumo Corp. as the applicant.

Decided510(k)DeviceDevice type
13 Oct 2004K040783FOUNDATIONLYC Synthetic Bone Grafting Material

Some of these clearances are listed with FDA today by another company: GC America Inc. (1).

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.