Neoss, Ltd. - FDA 510(k) Cleared Devices

Neoss, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2022. Active since 2005. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Neoss, Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Msquared Associates, Inc. and M Sqaured Associates, Inc..