Simpleware, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Simpleware, Ltd. makes
Simpleware, Ltd. produces image processing software, specifically the ScanIP, ScanIP: Medical Edition, and ScanIP: Med platforms. These products are used for the visualization and analysis of medical imaging data.
The company is based in the United States, and its portfolio includes Class II medical devices. These devices are listed in the FDA 510(k) regulatory registry.
Catalogue
Scanip; Scanip: Medical Edition; Scanip: Med Ref K142779
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Simpleware, Ltd. have in the registry?
The registry currently lists 1 device for Simpleware, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Simpleware, Ltd.'s devices?
Among its 1 most recently registered device, Simpleware, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Simpleware, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Simpleware, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Simpleware, Ltd. in the registry?
The most recently registered devices listed for Simpleware, Ltd. include SCANIP; SCANIP: MEDICAL EDITION; SCANIP: MED.