Scudder Molner Instruments
Country not established
- Devices
- 1
What Scudder Molner Instruments makes
Scudder Molner Instruments manufactures The Bionic Exerciser, a Class II medical device designed for physical rehabilitation or exercise purposes, likely incorporating mechanical or electromechanical components to assist movement or resistance training.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is based in the United States.
Catalogue
The Bionic Exerciser Ref K790746
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scudder Molner Instruments have in the registry?
The registry currently lists 1 device for Scudder Molner Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scudder Molner Instruments's devices?
Among its 1 most recently registered device, Scudder Molner Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Scudder Molner Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Scudder Molner Instruments's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scudder Molner Instruments in the registry?
The most recently registered devices listed for Scudder Molner Instruments include THE BIONIC EXERCISER.