Ultradent Product, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ultradent Product, Inc. has 2 FDA 510(k) cleared medical devices. Based in South Jordan, US.
Last cleared in 2023. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ultradent Product, 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.
2 devices