Fin-Ceramica Faenza S.p.A.
ItalyFDA applicant, unverified
- Devices
- 5
What Fin-Ceramica Faenza S.p.A. makes
Fin-Ceramica Faenza S.P.A. makes the CustomizedBone Service, which is a patient-specific bone implant or prosthetic device designed for individual anatomical needs.
The CustomizedBone Service is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
CustomizedBone Service Ref K160707
Regimes: 510(k) Registry: 510(k)CustomizedBone Service Ref K240567
Regimes: 510(k) Registry: 510(k)CustomizedBone Service Ref K193547
Regimes: 510(k) Registry: 510(k)CustomizedBone Service Ref K180513
Regimes: 510(k) Registry: 510(k)CustomizedBone Service Ref K171507
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fin-Ceramica Faenza S.P.A. have in the registry?
The registry currently lists 5 devices for Fin-Ceramica Faenza S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fin-Ceramica Faenza S.P.A.'s devices?
Among its 5 most recently registered devices, Fin-Ceramica Faenza S.P.A. has devices listed in FDA 510(k) (5 devices).
What risk classes do Fin-Ceramica Faenza S.P.A.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Fin-Ceramica Faenza S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fin-Ceramica Faenza S.P.A. in the registry?
The most recently registered devices listed for Fin-Ceramica Faenza S.P.A. include CustomizedBone Service.