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Kyocera Medical Technologies, Inc.

16 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar Anchor System (K261353)Kyocera Medical Technologies, Inc.2026-07-15
Tesera-k SC System (K242928)Kyocera Medical Technologies, Inc.2025-04-10
Initia T3 Acetabular Hemispherical Shell System (K242045)Kyocera Medical Technologies, Inc.2025-04-10
Tesera-k PL System and Tesera-k XL System (K242771)Kyocera Medical Technologies, Inc.2025-03-20
Initia Knee System (K243295)Kyocera Medical Technologies, Inc.2025-01-13
Skyway Anterior Cervical Plate System (K243015)Kyocera Medical Technologies, Inc.2024-11-05
TRIBRID® Unicompartmental Knee System (K232114)Kyocera Medical Technologies, Inc.2024-04-04
PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System (K230808)Kyocera Medical Technologies, Inc.2023-04-21
Tesera-K SC System (K223105)Kyocera Medical Technologies, Inc.2022-12-22
Tesera-k ALIF System (K212980)Kyocera Medical Technologies, Inc.2022-01-07
KMTI S141 Lumbar Interbody Fusion System (K212070)Kyocera Medical Technologies, Inc.2021-08-30
KMTI Hip Replacement System (K203472)Kyocera Medical Technologies, Inc.2021-04-02
KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System (K201660)Kyocera Medical Technologies, Inc.2020-07-16
Kyocera Bipolar Hip System (K200709)Kyocera Medical Technologies, Inc.2020-04-17
Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System (K200328)Kyocera Medical Technologies, Inc.2020-03-11
KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System (K193320)Kyocera Medical Technologies, Inc.2020-02-04

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Every clearance here is in the API, with alerts when new ones post.