Not currently registered with FDA under this name

Kinetic Instruments, Inc.

Bethel, CT, United States. Named as applicant on 2 dental 510(k) clearances between 2001 and 2002. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22001–2002
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Kinetic Instruments, Inc. as the applicant.

Decided	510(k)	Device	Device type
18 Oct 2002	K022862	TRANSCURE, MODEL 2910	EBZ Ultraviolet Activator for Polymerization
2 Oct 2001	K012946	SUNLITELED MODEL #2810	EBZ Ultraviolet Activator for Polymerization

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.