Skip to the page

Data / Medical devices / United Kingdom / Digital Surgery Limited

Digital Surgery Limited: FDA-registered device maker in London London, City of, United Kingdom, 1 510(k) clearance

Digital Surgery Limited is registered with the FDA (registration 3017296423) in London London, City of, United Kingdom. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 4, 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
3017296423
Address
230 City Rd, London London, City of, United Kingdom, EC1V 2QY
Owner or operator
Covidien llc (1282497)
Roles
Manufacturer
First device listed
September 10, 2026
Registered through
2026
Brand names listed
Instrument Exit Point on Touch Surgery™ Aide

Devices it lists

DeviceProduct codeClassRoleSource
Endoscopic Video Imaging System / Software Component For Real Time Video AugmentationSFE2Manufactureraccessdata.fda.gov
Software Controlled Endoscope And Instrument HolderQZB2Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 4, 2026K253984Instrument Exit Point on Touch Surgery™ AideSFESubstantially EquivalentCovidien, LLCaccessdata.fda.gov

Compare with other makers

Updated June 4, 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.