Maryrose
Country not established
- Devices
- 1
What Maryrose makes
Maryrose manufactures integrated movement analyzers, which assess biomechanical data for clinical or research applications. These devices capture motion metrics to support gait analysis, rehabilitation tracking, or sports performance evaluation.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Integrated Movement Analyzer Ref K944787
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maryrose have in the registry?
The registry currently lists 1 device for Maryrose. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maryrose's devices?
Among its 1 most recently registered device, Maryrose has devices listed in FDA 510(k) (1 device).
What risk classes do Maryrose's devices fall under?
Among its 1 most recently registered device, the classes recorded for Maryrose's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maryrose in the registry?
The most recently registered devices listed for Maryrose include INTEGRATED MOVEMENT ANALYZER.