Kyocera Medical Technologies Inc. (KMTI) - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Kyocera Medical Technologies Inc. (KMTI) has 2 FDA 510(k) cleared medical devices. Based in Redlands, US.
Latest FDA clearance: Apr 2025. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kyocera Medical Technologies Inc. (KMTI) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kyocera Medical Technologies Inc. (KMTI)
2 devices