Perspectum
United KingdomFDA applicant, unverified
Part of Perspectum, Ltd.
Perspectum is a medical device manufacturer, with 20 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 20
Registry facts
- Registries
- FDA GUDID 17
- FDA 510(k) 3
- Device classes
- FDA Class II 20
- Sites and related companies
What Perspectum makes
Perspectum develops software applications for radiology and MRI systems, including tools for processing DICOM images and enhancing liver and biliary imaging. Key products include specialized MRI software for liver analysis (e.g., LiverMultiScan), biliary duct visualization (MRCP+), and automated image coverage mapping (CoverScan, VitruvianScan). Additional offerings focus on liver-specific diagnostic support (Hepatica).
The company’s portfolio is regulated under FDA Class II devices and appears in the FDA’s 510(k) and UDI registries. Products are listed under radiology and MRI software categories, adhering to U.S. medical device compliance requirements.
Catalogue
Search and filter all 20 devicesFrequently asked questions
How many devices does Perspectum have in the registry?
The registry currently lists 20 devices for Perspectum. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perspectum's devices?
Among its 20 most recently registered devices, Perspectum has devices listed in FDA 510(k) (3 devices) and FDA GUDID (17 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Perspectum's devices fall under?
Among its 20 most recently registered devices, the classes recorded for Perspectum's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perspectum in the registry?
The most recently registered devices listed for Perspectum include LiverMultiScan 5.0.0, LiverMultiScan 3.2.0, CoverScan 1.0.0 and LiverMultiScan 3.1.0.