Not currently registered with FDA under this name

Ardent Production Development

Tonawanda, NY, United States. Named as applicant on 2 dental 510(k) clearances between 1996 and 1997. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21996–1997
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Ardent Production Development as the applicant.

Decided	510(k)	Device	Device type
6 Jan 1997	K964192	ARDENT NON GAMMA-2 70	EJJ Amalgam Alloy
10 Dec 1996	K964775	ARDENT FUTURA NON GAMMA-2	EJJ Amalgam Alloy

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.