Medadonics, Inc.
Country not established
- Devices
- 1
What Medadonics, Inc. makes
Medadonics, Inc. manufactures the ULTRASOUND STETHOSCOPE® INTRADOP®, a device designed for enhanced auscultation with ultrasound integration to improve diagnostic accuracy during patient monitoring.
The company’s portfolio is regulated under FDA’s Class II device classification, with the ULTRASOUND STETHOSCOPE® INTRADOP® listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Ultrasound Stethoscope(R) Intradop(R) Ref K912033
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medadonics, Inc. have in the registry?
The registry currently lists 1 device for Medadonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medadonics, Inc.'s devices?
Among its 1 most recently registered device, Medadonics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medadonics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medadonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medadonics, Inc. in the registry?
The most recently registered devices listed for Medadonics, Inc. include ULTRASOUND STETHOSCOPE(R) INTRADOP(R).