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Data / Medical devices / Oximeter / United Kingdom

FDA-registered makers of Oximeter in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Oximeter (product code DQA). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Oximeter
Product code
DQA
Country
United Kingdom

Makers of Oximeter in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Huntleigh Healthcare Ltd.Cardiff, South Glamorgan, United KingdomComplaint file establishment, Manufacturer1October 1, 2008000api.fda.gov
Surepulse Medical LimitedNottingham Nottinghamshire, United KingdomExporter to the US, Specification developer1July 23, 2021010api.fda.gov
Current Health LtdEdinburgh Edinburgh, City of, United KingdomSpecification developer0000api.fda.gov
Dynamic Ems LtdDalgety Bay Fife, United KingdomContract manufacturer0000api.fda.gov
Key-Tech Scotland LtdDunfermline Fife, United KingdomContract manufacturer0000api.fda.gov
Remote Diagnostic Technologies Ltd.FARNBOROUGH Hampshire, United KingdomComplaint file establishment, Manufacturer0000api.fda.gov
Tioga LimitedDERBY Derbyshire, United KingdomContract manufacturer0000api.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.