Not currently registered with FDA under this name

3DBiocad

Renton, WA, United States. 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 3DBiocad as the applicant.

Decided	510(k)	Device	Device type
13 May 2020	K193055	Purzir Dental Zirconia	EIH Porcelain Powder

Some of these clearances are listed with FDA today by another company: Seattle Bioceramics, Inc. (1).

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.