Medison America, Inc.
United StatesFDA applicant, unverified
- Devices
- 21
What Medison America, Inc. makes
Medison America, Inc. manufactures diagnostic ultrasound systems and transducers, including models like the MYCOLOR 202, SA8800, and SONOACE series. These systems are designed for medical imaging applications, such as abdominal, small parts, and endorectal scans, with specialized probes like the Volusion abdominal and endorectal transducers.
The company’s products are classified as Class II medical devices under FDA regulations and are recorded in the 510(k) clearance database. The manufacturer is based in the United States.
Catalogue
Search and filter all 21 devicesFrequently asked questions
How many devices does Medison America, Inc. have in the registry?
The registry currently lists 21 devices for Medison America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medison America, Inc.'s devices?
Among its 21 most recently registered devices, Medison America, Inc. has devices listed in FDA 510(k) (21 devices).
What risk classes do Medison America, Inc.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Medison America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medison America, Inc. in the registry?
The most recently registered devices listed for Medison America, Inc. include MYCOLOR 202 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS, SA8800 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS,, SONOACE 6000C DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS, ALSO CALLED ULTRASOUND SYSTEM AND TRANSDUCERS and SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM.