Not currently registered with FDA under this name

Revisios BV

3723 Mb Bilthoven, Netherlands. Named as applicant on 1 dental 510(k) clearance between 2020 and 2020. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12020–2020
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Revisios BV as the applicant.

Decided	510(k)	Device	Device type
2 Oct 2020	K201546	OsOpia Synthetic Bone Void Filler	LYC Synthetic Bone Grafting 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.