Kyocera Medical Technologies, Inc.
FDA 510(k) medical device clearances.
Top product codes for Kyocera Medical Technologies, Inc.
Recent clearances by Kyocera Medical Technologies, Inc.
- 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.