Straumann Institute, Ltd.
Country not established
- Devices
- 1
What Straumann Institute, Ltd. makes
The company produces accessories and instruments for the BONEFIT Implant System, including tools and components designed to support dental implant procedures.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Bonefit Implant System Accessories & Instruments Ref K894844
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Straumann Institute, Ltd. have in the registry?
The registry currently lists 1 device for Straumann Institute, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Straumann Institute, Ltd.'s devices?
Among its 1 most recently registered device, Straumann Institute, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Straumann Institute, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Straumann Institute, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Straumann Institute, Ltd. in the registry?
The most recently registered devices listed for Straumann Institute, Ltd. include BONEFIT IMPLANT SYSTEM ACCESSORIES & INSTRUMENTS.