Mechanodontics, Inc.
Country not established
- Devices
- 1
What Mechanodontics, Inc. makes
Mechanodontics, Inc. develops the BRUIS Software Suite, a digital tool designed for analyzing and assessing musculoskeletal injuries and rehabilitation progress through biomechanical data collection and reporting.
The BRUIS Software Suite is classified as a Class II medical device in the US and is listed under FDA’s 510(k) clearance pathway. The company is based in the United States.
Catalogue
BRUIS Software Suite Ref K191720
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mechanodontics, Inc. have in the registry?
The registry currently lists 1 device for Mechanodontics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mechanodontics, Inc.'s devices?
Among its 1 most recently registered device, Mechanodontics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mechanodontics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mechanodontics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mechanodontics, Inc. in the registry?
The most recently registered devices listed for Mechanodontics, Inc. include BRUIS Software Suite.