Msi France
FranceFDA applicant, unverified
- Devices
- 1
What Msi France makes
Msi France manufactures the SPI Dental Implant System, a dental implant solution designed for osseointegration in oral and maxillofacial applications.
The SPI Dental Implant System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
SPI Dental Implant System Ref K172240
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Msi France have in the registry?
The registry currently lists 1 device for Msi France. Devices recorded under merged duplicate company entries are counted once.
Which registries list Msi France's devices?
Among its 1 most recently registered device, Msi France has devices listed in FDA 510(k) (1 device).
What risk classes do Msi France's devices fall under?
Among its 1 most recently registered device, the classes recorded for Msi France's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Msi France in the registry?
The most recently registered devices listed for Msi France include SPI Dental Implant System.