Not currently registered with FDA under this name

Dentron, Inc.

Mchenry, IL, United States. Named as applicant on 2 dental 510(k) clearances between 1982 and 1982. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21982–1982
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Dentron, Inc. as the applicant.

Decided	510(k)	Device	Device type
10 Jun 1982	K820998	DENTRON-DIRECT-TRAY	EBH Resin Impression Tray Material
10 Jun 1982	K820997	DENTRON-EXACT - TRAY	EBH Resin Impression Tray Material

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.