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Data / Medical devices / System, Image Processing, Radiological / United Kingdom

FDA-registered makers of System, Image Processing, Radiological in the United Kingdom: 14 establishments

14 establishments in the United Kingdom are registered with the FDA to make System, Image Processing, Radiological (product code LLZ). 14 have a 510(k) clearance or PMA approval on file and 1 has a recall event. 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.

Get makers of this device in the United KingdomWatch these makers
Device
System, Image Processing, Radiological
Product code
LLZ
Country
United Kingdom

Makers of System, Image Processing, Radiological in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Brainomix LimitedOxford Oxfordshire, United KingdomComplaint file establishment, Manufacturer4January 6, 2025000api.fda.gov
Mirada Medical LimitedOxford (UK) Oxfordshire, United KingdomManufacturer4April 15, 2022000api.fda.gov
Claritas Healthtech LimitedLondon London, City of, United KingdomManufacturer3August 5, 2025000api.fda.gov
Perspectum Ltd.Oxford Oxfordshire, United KingdomManufacturer3March 13, 2024000api.fda.gov
Axial Medical Printing LimitedBelfast, United KingdomManufacturer2January 24, 2024000api.fda.gov
Icat Solutions LtdNorwich Norfolk, United KingdomComplaint file establishment, Manufacturer2April 8, 2025000api.fda.gov
Meridian Technique LtdSOUTHAMPTON Hampshire, United KingdomManufacturer2October 18, 2017000api.fda.gov
Simpleware Product Group, SYNOPSYS NORTHERN EUROPEExeter Devon, United KingdomComplaint file establishment, Manufacturer2April 1, 2021010api.fda.gov
Blackford Analysis LtdEDINBURGH Midlothian, United KingdomManufacturer1March 19, 2015000api.fda.gov
Biotronics 3D LimitedLondon London, City of, United KingdomManufacturer1April 24, 2024000api.fda.gov
Caristo DiagnosticsOxford Oxfordshire, United KingdomManufacturer1February 20, 2025000api.fda.gov
Corin LimitedCIRENCESTER Gloucestershire, United KingdomComplaint file establishment, Manufacturer1January 7, 2025000api.fda.gov
Motilent LtdLondon England, United KingdomComplaint file establishment, Manufacturer1November 8, 2021000api.fda.gov
Mycardium Ai LtdLiverpool, United KingdomComplaint file establishment, Manufacturer1November 15, 2024000api.fda.gov

Updated November 2, 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.