Kyocera Medical Corporation
JapanFDA applicant, unverified FDA FEI 3010566635
- Devices
- 574
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
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.
Catalogue
Search and filter all 574 devicesShowing 1-50 of 574
Company details
- FDA FEI number
- 3010566635
- DUNS number
- 691363290
- Address
- 6 Takeda Tobadono-cho, Fushimi-ku, Kyoto
- [email protected]
- Phone
- 909-557-2360
Frequently asked questions
How many devices does Kyocera Medical Corporation have in the registry?
The registry currently lists 574 devices for Kyocera Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kyocera Medical Corporation's devices?
Among its 50 most recently registered devices, Kyocera Medical Corporation has devices listed in FDA GUDID (50 devices).
What risk classes do Kyocera Medical Corporation's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Kyocera Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kyocera Medical Corporation in the registry?
The most recently registered devices listed for Kyocera Medical Corporation include Initia Total Hip System GMH02-100001, Initia Total Hip System GMH02-100002, Initia Total Hip System GMH02-100003 and Initia Total Hip System GMH02-100004.