Creodent Prosthetics, Ltd. - FDA 510(k) Cleared Devices

Creodent Prosthetics, Ltd. has 9 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2022. Active since 2013. Primary specialty: Dental.

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

Regulatory submissions have been managed by Aclivi, LLC and Withus Group, Inc..