Mendaera, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mendaera, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Mateo, US.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mendaera, Inc. Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
1 devices