Not currently registered with FDA under this name

Techmah Cmf

Knoxville, TN, United States. Named as applicant on 2 dental 510(k) clearances between 2023 and 2024. No establishment is registered with FDA under this exact name today.

2 clearances in five years

Device types listed: 0
Brands and models: 0
510(k) clearances: 22023–2024
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Techmah Cmf as the applicant.

Decided	510(k)	Device	Device type
11 Jul 2024	K233874	tmCMF Solution	JEY Bone Plate
2 Oct 2023	K231520	tmCMF Solution	DZJ Manual Wire Driver and Bone Drill

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.