Kyocera America, Inc.
Country not established
- Devices
- 1
What Kyocera America, Inc. makes
Kyocera America, Inc. manufactures dental implants under the Bioceram series, specifically the Series II, designed for osseointegration in oral and maxillofacial applications.
The Bioceram Series II dental implants are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Bioceram Dental Implant, Series Ii Ref K904450
510(k) 510(k)
Frequently asked questions
How many devices does Kyocera America, Inc. have in the registry?
The registry currently lists 1 device for Kyocera America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kyocera America, Inc.'s devices?
Among its 1 most recently registered device, Kyocera America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kyocera America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kyocera America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kyocera America, Inc. in the registry?
The most recently registered devices listed for Kyocera America, Inc. include BIOCERAM DENTAL IMPLANT, SERIES II.