Not currently registered with FDA under this name

Immediateload S.A.

Agno, Switzerland. Named as applicant on 1 dental 510(k) clearance between 2016 and 2016. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12016–2016
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Immediateload S.A. as the applicant.

Decided	510(k)	Device	Device type
3 Aug 2016	K151757	IMMEDIATELOAD Dental Implant System	DZE Root-Form Endosseous Implant

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.