Not currently registered with FDA under this name

Matrix Surgical Holdings, LLC/Matrix Surgical USA

Atlanta, GA, United States. Named as applicant on 1 dental 510(k) clearance between 2018 and 2018. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12018–2018
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Matrix Surgical Holdings, LLC/Matrix Surgical USA as the applicant.

Decided	510(k)	Device	Device type
11 Oct 2018	K180249	OmniPore DUROMAX Surgical Implants	JEY Bone Plate

Some of these clearances are listed with FDA today by another company: Matrix Surgical Holdings, LLC. dba Matrix Surgical USA (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.