Dental Device Guide
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Not currently registered with FDA under this name

Arent Fox

Washington, DC, United States. Named as applicant on 1 dental 510(k) clearance between 1995 and 1995. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11995–1995
Markets registered in
1United States
Establishments
0—
1995: 11990200020102020

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Arent Fox as the applicant.

Decided510(k)DeviceDevice type
11 Jul 1995K945843SAFETY PLUSEJI Cartridge Syringe

Some of these clearances are listed with FDA today by another company: Septodont (1), Sofic (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.