Data / Medical devices / United Kingdom / Perspectum Ltd.
Perspectum Ltd.: FDA-registered device maker in Oxford Oxfordshire, United Kingdom, 9 510(k) clearances
Perspectum Ltd. is registered with the FDA (registration 3014232555) in Oxford Oxfordshire, United Kingdom. It lists 2 device types. The FDA files 9 510(k) clearances under its listings, the newest dated March 9, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3014232555
- Address
- Gemini One 5520 John Smith Drive, Oxford Oxfordshire, United Kingdom, OX4 2LL
- Owner or operator
- Perspectum Ltd. (10056574)
- Roles
- Manufacturer
- First device listed
- December 22, 2017
- Registered through
- 2026
- Brand names listed
- CoverScan, Hepatica, Hepatica v1, LMSv3, LiverMultiScan, LiverMutliScan, MRCP+v1, VitruvianScan
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Manufacturer | accessdata.fda.gov |
| System, Nuclear Magnetic Resonance Imaging | LNH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 9, 2026 | K253413 | LiverMultiScan (v6.0) | LNH | Substantially Equivalent | Perspectum, Ltd. | accessdata.fda.gov |
| October 2, 2024 | K241925 | VitruvianScan (v1.0) | LNH | Substantially Equivalent | Perspectum, Ltd. | accessdata.fda.gov |
| March 13, 2024 | K233930 | MRCP+ version 2 (MRCP+ v2) | LLZ | Substantially Equivalent | Perspectum | accessdata.fda.gov |
| September 6, 2022 | K213960 | LiverMultiScan v5 (LMSv5) | LNH | Substantially Equivalent | Perspectum | accessdata.fda.gov |
| May 19, 2022 | K212565 | CoverScan v1 | LLZ | Substantially Equivalent | Perspectum, Ltd. | accessdata.fda.gov |
| January 12, 2021 | K203280 | Hepatica v1 (Hepatica v1.0.0) | LNH | Substantially Equivalent | Perspectum, Ltd. | accessdata.fda.gov |
| June 27, 2019 | K190017 | LiverMultiScan (LMSv3) | LNH | Substantially Equivalent | Perspectum Diagnostics, Ltd. | accessdata.fda.gov |
| January 9, 2019 | K183133 | MRCP+ v1.0 | LLZ | Substantially Equivalent | Perspectum Diagnostics, Ltd. | accessdata.fda.gov |
| November 21, 2017 | K172685 | LiverMultiScan | LNH | Substantially Equivalent | Perspectum Diagnostics, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Nuclear Magnetic Resonance Imaging
- All makers of System, Image Processing, Radiological
Updated March 9, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.