Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Kyocera Medical Technologies Inc. (KMTI)

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest FDA decision2026-05-15
TypeNumberDevice NameCodeDateActions
510(k) K260989 Varion Thoracolumbar Fixation SystemNKB2026-05-15 View
510(k) K250486 Skyway Anterior Cervical Plate SystemKWQ2025-04-10 View
510(k) K231766 Skyway Anterior Cervical Plate SystemKWQ2023-09-12 View
↑