Kyocera Medical Technologies, Inc.
Kyocera Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2026.
Top product codes for Kyocera Medical Technologies, Inc.
Recent clearances by Kyocera Medical Technologies, Inc.
- K261353 — Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar Anchor System
- K242045 — Initia T3 Acetabular Hemispherical Shell System
- K242928 — Tesera-k SC System
- K242771 — Tesera-k PL System and Tesera-k XL System
- K243295 — Initia Knee System
- K243015 — Skyway Anterior Cervical Plate System
- K232114 — TRIBRID® Unicompartmental Knee System
- K230808 — PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System
- K223105 — Tesera-K SC System
- K212980 — Tesera-k ALIF System
- K212070 — KMTI S141 Lumbar Interbody Fusion System
- K203472 — KMTI Hip Replacement System
- K201660 — KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System
- K200709 — Kyocera Bipolar Hip System
- K200328 — Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System
- K193320 — KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System
Data sourced from openFDA. This site is unofficial and independent of the FDA.