Guidemia Technologies, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Guidemia Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Cypress, US.
Historical record: 2 cleared submissions from 2012 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Guidemia Technologies, LLC Filter by specialty or product code using the sidebar.
2 devices