Archform, Inc. - FDA 510(k) Cleared Devices

Archform, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bakersfield, US.

Last cleared in 2021. Active since 2021. Primary specialty: Dental.

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

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.