Vibronics
Country not established
- Devices
- 1
What Vibronics makes
Vibronics makes the Vibronics Auto Core Biopsy Device (ACBD), a medical device used for obtaining tissue samples during biopsy procedures.
The Vibronics Auto Core Biopsy Device is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Vibronics Auto Core Biopsy Device (Acbd) Ref K904987
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vibronics have in the registry?
The registry currently lists 1 device for Vibronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vibronics's devices?
Among its 1 most recently registered device, Vibronics has devices listed in FDA 510(k) (1 device).
What risk classes do Vibronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vibronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vibronics in the registry?
The most recently registered devices listed for Vibronics include VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD).