Dental Device Guide
Add your company

Not currently registered with FDA under this name

Tekka

Bethesda, MD, United States. Named as applicant on 2 dental 510(k) clearances between 2003 and 2003. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
22003–2003
Markets registered in
1United States
Establishments
0—
2003: 2200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Tekka as the applicant.

Decided510(k)DeviceDevice type
12 Nov 2003K032520ORTRAUTEK TRAUMA SYSTEMJEY Bone Plate
28 Oct 2003K031989ORTRAUTEK ORTHOGNATHIC SYSTEMJEY Bone Plate

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.