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Kyocera Medical Corporation

JapanFDA applicant, unverified FDA FEI 3010566635

Devices
574
Registrations
FDA
FDA recalls
0

What Kyocera Medical Corporation makes

Kyocera Medical Corporation manufactures orthopedic implants, including the Initia Total Hip System and BIOCERAM AZUL® ceramic femoral heads, designed for primary total hip arthroplasty procedures.

These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Company details

FDA FEI number
3010566635
DUNS number
691363290
Address
6 Takeda Tobadono-cho, Fushimi-ku, Kyoto
Phone
909-557-2360