Dental Device Guide
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Not currently registered with FDA under this name

Biosoft International Corp.

Trenton, NJ, United States. Named as applicant on 1 dental 510(k) clearance between 2000 and 2000. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12000–2000
Markets registered in
1United States
Establishments
0—
2000: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Biosoft International Corp. as the applicant.

Decided510(k)DeviceDevice type
23 Jun 2000K001640BIOSOFT RESINEBI Rebasing Repairing Relining Denture Resin

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.