Rind Medical Development
Country not established
- Devices
- 1
What Rind Medical Development makes
Rind Medical Development manufactures the RIND AIRWAY, a medical device designed for airway management in clinical settings.
The RIND AIRWAY is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Rind Airway Ref K812822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rind Medical Development have in the registry?
The registry currently lists 1 device for Rind Medical Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rind Medical Development's devices?
Among its 1 most recently registered device, Rind Medical Development has devices listed in FDA 510(k) (1 device).
What risk classes do Rind Medical Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rind Medical Development's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rind Medical Development in the registry?
The most recently registered devices listed for Rind Medical Development include RIND AIRWAY.