Davis Medical
Country not established
- Devices
- 3
What Davis Medical makes
Davis Medical manufactures the RHINOGUARD, a nasal device designed to protect against foreign objects or trauma during medical procedures.
The RHINOGUARD is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Rhinoguard Ref K141747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Davis Medical have in the registry?
The registry currently lists 3 devices for Davis Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Davis Medical's devices?
Among its 3 most recently registered devices, Davis Medical has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Davis Medical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Davis Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Davis Medical in the registry?
The most recently registered devices listed for Davis Medical include RhinoGuard™ Small, RhinoGuard™ Large and RHINOGUARD.