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Kyocera Medical Technologies Inc. (KMTI)

FDA Regulatory Profile

Kyocera Medical Technologies Inc. (KMTI) appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 15, 2026.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260989Varion Thoracolumbar Fixation SystemMay 15, 2026
K250486Skyway Anterior Cervical Plate SystemApril 10, 2025
K231766Skyway Anterior Cervical Plate SystemSeptember 12, 2023

FDA data resources