Not currently registered with FDA under this name

Televere Systems, Inc.

Arnold, MD, 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 Televere Systems, Inc. as the applicant.

Decided	510(k)	Device	Device type
20 Jun 2018	K181358	Televere Digital Dental Imaging System	MUH Digital Extraoral Source X-Ray System

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.