Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 9 of 12
DeviceModel / ReferenceRegistriesClassStatus
Initia Total Hip System GMH02-200133
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500020
FDA UDI
Class IIActive
Initia Total Hip System TJ41394-49
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400012
FDA UDI
Class IIActive
Initia Total Hip System TJ33122
FDA UDI
Class IIActive
Initia Total Hip System TJ33674
FDA UDI
Class IIActive
Initia Total Hip System TJ39953-1
FDA UDI
Class IIActive
Initia Total Hip System TJ51146-2
FDA UDI
Class IUnknown
Initia Total Hip System TJ40394
FDA UDI
Class IActive
Initia Total Hip System TJ39954-1
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100052
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200049
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200061
FDA UDI
Class IIActive
Initia Total Hip System GMH06-900018
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200050
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100013
FDA UDI
Class IIActive
Initia Total Hip System 1183-6007-01
FDA UDI
Class IIActive
Initia Total Hip System TJ34360-1
FDA UDI
Class IActive
Initia Total Hip System TJ36137-1
FDA UDI
Class IActive
Initia Total Hip System GMH02-500029
FDA UDI
Class IIActive
Bioceram Azul Head GMH04-400060
FDA UDI
Class IIActive
Initia Total Hip System TJ41394-21
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-19
FDA UDI
Class IIActive
Initia Total Hip System TJ39991-1
FDA UDI
Class IActive
Initia Total Hip System GMH02-200188
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500036
FDA UDI
Class IIActive
Initia Total Hip System TJ41394-26
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200055
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400005
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200013
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200063
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-44
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200084
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200143
FDA UDI
Class IIActive
Initia Total Hip System GMH02-500015
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200202
FDA UDI
Class IIActive
Initia Total Hip System TJ34624
FDA UDI
Class IActive
Initia Total Hip System TJ33442-7
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400019
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200200
FDA UDI
Class IIActive
Initia Total Hip System TJ41392-50
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200010
FDA UDI
Class IIActive
Bioceram Azul Head GMH04-400072
FDA UDI
Class IIActive
Initia Total Hip System GMH02-100016
FDA UDI
Class IIActive
Bioceram Azul Head GMH04-400053
FDA UDI
Class IIActive
Initia Total Hip System GMH02-200023
FDA UDI
Class IIActive
Initia Total Hip System TJ41393-21
FDA UDI
Class IIActive
Initia Total Hip System 21057-00-0000
FDA UDI
Class IIActive
Initia Total Hip System GMH03-400003
FDA UDI
Class IIActive
Initia Total Hip System TJ41391-21
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.