Dunhall Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Dunhall Pharmaceuticals, Inc. makes
Dunhall Pharmaceuticals, Inc. manufactures DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURS, which are Class I medical devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Dunhall/Omnii International Rotary Diamond Burs Ref K940908
510(k) 510(k)
Frequently asked questions
How many devices does Dunhall Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Dunhall Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dunhall Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Dunhall Pharmaceuticals, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dunhall Pharmaceuticals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dunhall Pharmaceuticals, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dunhall Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Dunhall Pharmaceuticals, Inc. include DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURS.