Accudent, Inc.
Country not established
- Devices
- 1
What Accudent, Inc. makes
Accudent, Inc. manufactures the ACCUDENT ACCUPROBE, a device designed for precise measurement or testing in medical or diagnostic applications, though specific use cases are not detailed.
The ACCUPROBE is classified as a Class I medical device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States.
Catalogue
Accudent Accuprobe Ref K870280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accudent, Inc. have in the registry?
The registry currently lists 1 device for Accudent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accudent, Inc.'s devices?
Among its 1 most recently registered device, Accudent, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Accudent, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Accudent, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Accudent, Inc. in the registry?
The most recently registered devices listed for Accudent, Inc. include ACCUDENT ACCUPROBE.