Skip to the page

Data / Medical devices / Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use / United Kingdom

FDA-registered makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in the United Kingdom: 5 establishments

5 establishments in the United Kingdom are registered with the FDA to make Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use (product code LXG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 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.

Device
Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Product code
LXG
Country
United Kingdom

Makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Apacor LimitedWokingham, Berkshire, United KingdomExporter to the US, Manufacturer0000api.fda.gov
Bedfont Scientific Ltd.MAIDSTONE Kent, United KingdomManufacturer0000api.fda.gov
Cellpath LtdNEWTOWN Powys, United KingdomSpecification developer0000api.fda.gov
Immunodiagnostic Systems Ltd.Boldon Colliery Durham, United KingdomManufacturer0000api.fda.gov
Medical Wire And Equipment Co. Ltd.Corsham, Wiltshire, United KingdomManufacturer0000api.fda.gov

Updated November 3, 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.