Not currently registered with FDA under this name

Rms Div.

Amherst, NY, United States. Named as applicant on 3 dental 510(k) clearances between 1994 and 1994. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31994–1994
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Rms Div. as the applicant.

Decided	510(k)	Device	Device type
14 Dec 1994	K944848	THE VIVACARE T.P.S. PROBE	EIX Periodontic Probe
3 Nov 1994	K944557	DW250 #91	EJT Gold-Based Noble Metal Alloy
22 Jun 1994	K941625	DW234 #29	EJS Alloy Other Noble Metal

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.