Kyocera Medical Technologies Inc. (KMTI) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kyocera Medical Technologies Inc. (KMTI) - FDA 510(k) Cleared Devices
Recent clearances: Varion Thoracolumbar Fixation System, Skyway Anterior Cervical Plate System, Skyway Anterior Cervical Plate System
3
Total
3
Cleared
0
Denied
Kyocera Medical Technologies Inc. (KMTI) has 3 FDA 510(k) cleared medical devices. Based in Redlands, US.
Latest FDA clearance: May 2026. 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.
Regulatory submissions have been managed by Empirical Technologies and Applied Technical Services (Empirical Technologies).
FDA 510(k) Regulatory Record - Kyocera Medical Technologies Inc. (KMTI)
3 devices