Ortivus US, Inc.
Country not established
- Devices
- 1
What Ortivus US, Inc. makes
Ortivus Us, Inc. manufactures the MOBIMED System, including the PEGASUS and POLARIS models, which are designed for medical imaging and diagnostic procedures. These systems appear to support mobile imaging solutions, likely for use in operating rooms or other clinical environments where portability is required.
The MOBIMED System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Mobimed System, (Pegasus And Polaris) Ref K973318
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ortivus Us, Inc. have in the registry?
The registry currently lists 1 device for Ortivus Us, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortivus Us, Inc.'s devices?
Among its 1 most recently registered device, Ortivus Us, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ortivus Us, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ortivus Us, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ortivus Us, Inc. in the registry?
The most recently registered devices listed for Ortivus Us, Inc. include MOBIMED SYSTEM, (PEGASUS AND POLARIS).