Mars Bioimaging, Ltd.
New ZealandFDA applicant, unverified
- Devices
- 1
What Mars Bioimaging, Ltd. makes
Mars Bioimaging, Ltd. manufactures an Extremity CT Imaging System designed for high-resolution imaging of peripheral bones and joints, enabling detailed visualization for diagnostic and surgical planning purposes.
The company’s product portfolio is regulated under Class II devices in the US and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Extremity CT Imaging System Ref K252249
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mars Bioimaging, Ltd. have in the registry?
The registry currently lists 1 device for Mars Bioimaging, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mars Bioimaging, Ltd.'s devices?
Among its 1 most recently registered device, Mars Bioimaging, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mars Bioimaging, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mars Bioimaging, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mars Bioimaging, Ltd. in the registry?
The most recently registered devices listed for Mars Bioimaging, Ltd. include Extremity CT Imaging System.