Not currently registered with FDA under this name

Clp Products

Lake Park, FL, United States. Named as applicant on 1 dental 510(k) clearance between 1996 and 1996. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11996–1996
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Clp Products as the applicant.

Decided	510(k)	Device	Device type
14 Feb 1996	K955528	CLP BONNET	DZB Orthodontic Extraoral Headgear

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.