Not currently registered with FDA under this name

Martin D. Lerman

Mchenry, IL, United States. Named as applicant on 1 dental 510(k) clearance between 1983 and 1983. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11983–1983
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Martin D. Lerman as the applicant.

Decided	510(k)	Device	Device type
12 Aug 1983	K831793	AQUALIZER MOUTHPIECE	KMY Preformed Tooth Positioner

Some of these clearances are listed with FDA today by another company: Jumar Corporation (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.