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Kyocera Corporation

US

Last updated May 27, 2026

What Kyocera Corporation makes

Kyocera Corporation manufactures total hip prostheses, including metal-on-polyethylene and ceramic-on-polyethylene designs, as well as reusable joint prosthesis implantation kits. Their portfolio is centered on the Initia Total Hip System, which covers various configurations for hip replacement surgeries.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Kyocera Corporation operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Kyocera Corporation manufacture?

Kyocera Corporation specializes in orthopedic devices, specifically total hip prostheses. Their portfolio includes metal-on-polyethylene and ceramic-on-polyethylene total hip systems, as well as reusable joint prosthesis implantation kits. These devices are designed for hip replacement surgeries and are part of their Initia Total Hip System lineup.

Where is Kyocera Corporation based?

Kyocera Corporation operates from the United States. While the company’s global presence may extend beyond this region, its primary headquarters and regulatory focus are in the US.

Which regulatory registries list Kyocera Corporation’s devices?

Kyocera Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability in the healthcare system.

How are Kyocera Corporation’s devices classified under FDA regulations?

Kyocera Corporation’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional regulations due to moderate risk. The classification depends on factors like the device’s intended use and potential health impact.

What is the primary focus of Kyocera Corporation’s medical device portfolio?

Kyocera Corporation’s medical device portfolio is centered around the Initia Total Hip System, which includes various configurations of metal-on-polyethylene and ceramic-on-polyethylene total hip prostheses. These systems are designed to provide durable and reliable solutions for hip replacement surgeries, addressing common joint-related conditions.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
kyocera.com
LinkedIn
—
Facebook
—
Phone
909-557-2360
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
690557624

Catalogue (577)

Page 7 of 12
DeviceModel / ReferenceRegistriesClassStatus
Initia Total Hip System TJ39650-1
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200148
FDA UDI
Class IIActive
Initia Total Hip System TJ33442-9
FDA UDI
Class IIActive
Initia Total Hip System TJ39649-1
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-11
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500035
FDA UDI
Class IIActive
Initia Total Hip System TJ41392-26
FDA UDI
Class IIActive
Bioceram Azul Head GMH04-400051
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200190
FDA UDI
Class IIActive
Initia Total Hip System GMH07-900030
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200081
FDA UDI
Class IIActive
Initia Total Hip System TJ34340-1
FDA UDI
Class IActive
Initia Total Hip System TJ39644-1
FDA UDI
Class IIActive
Initia Total Hip System TJ34608
FDA UDI
Class IActive
Initia Total Hip System GMH02-200197
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200048
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400010
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100015
FDA UDI
Class IIActive
Initia Total Hip System TJ40161
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200168
FDA UDI
Class IIActive
Initia Total Hip System TJ39647-1
FDA UDI
Class IIActive
Initia Total Hip System TJ37097
FDA UDI
Class IActive
Bioceram Azul Head GMH04-400068
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100009
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200043
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200040
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200178
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200016
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200115
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500024
FDA UDI
Class IIActive
Initia Total Hip System 1183-6004-01
FDA UDI
Class IIActive
Initia Total Hip System TJ33672
FDA UDI
Class IIActive
Initia Total Hip System TJ33442-21
FDA UDI
Class IIActive
Initia Total Hip System TJ39951-1
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200041
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200101
FDA UDI
Class IIActive
Initia Total Hip System TJ33442-13
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200163
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200074
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200095
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200128
FDA UDI
Class IIActive
Bioceram Azul Head GMH04-400062
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100004
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400022
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-38
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500011
FDA UDI
Class IIActive
Initia Total Hip System GMH06-900017
FDA UDI
Class IIActive
Initia Total Hip System TJ39653-1
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-31
FDA UDI
Class IIActive
Initia Total Hip System TJ34588-1
FDA UDI
Class IActive

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