Acroviz, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Acroviz, Inc. makes
Acroviz, Inc. manufactures the AcroDTI Visualizer, a device designed for diagnostic imaging in the assessment of deep tissue injuries, such as pressure ulcers or traumatic wounds.
The AcroDTI Visualizer is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
AcroDTI Visualizer Ref K201948
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acroviz, Inc. have in the registry?
The registry currently lists 1 device for Acroviz, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acroviz, Inc.'s devices?
Among its 1 most recently registered device, Acroviz, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Acroviz, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Acroviz, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acroviz, Inc. in the registry?
The most recently registered devices listed for Acroviz, Inc. include AcroDTI Visualizer.