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Data / Medical devices / United Kingdom / Vision RT Ltd

Vision RT Ltd: FDA-registered device maker in Basingstoke Hampshire, United Kingdom, 8 510(k) clearances

Vision RT Ltd is registered with the FDA (registration 3014428919) in Basingstoke Hampshire, United Kingdom. It lists 2 device types. The FDA files 8 510(k) clearances under its listings, the newest dated March 18, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3014428919
Address
Jays Close Viables Industrial Estate, Basingstoke Hampshire, United Kingdom, RG22 4BS
Owner or operator
VISION RT LIMITED (9063759)
Roles
Complaint file establishment, Manufacturer
First device listed
February 2, 2006
Registered through
2026
Brand names listed
ALIGNRT, AlignRT, AlignRT Advance, AlignRT InBore, AlignRT Offline, AlignRT Plus, AlignRT SRS module, AlignRT system and more

Devices it lists

DeviceProduct codeClassRoleSource
Accelerator, Linear, MedicalIYE2Complaint file establishment, Manufactureraccessdata.fda.gov
Medical Device Data SystemOUG1Manufactureraccessdata.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
March 18, 2026K253012AlignRT Plus (8.0)IYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
May 19, 2025K243301MapRTIYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
March 29, 2024K233622AlignRT PlusIYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
November 10, 2021K212583AlignRT PlusIYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
March 4, 2021K203387AlignRT PlusIYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
January 8, 2013K123371ALIGNRT PLUSIYESubstantially EquivalentVision RT Limitedaccessdata.fda.gov
October 1, 2007K072171GATECT-RTIYESubstantially EquivalentVision RT Limitedaccessdata.fda.gov
January 6, 2006K052682ALIGNRTIYESubstantially EquivalentVision RT Limitedaccessdata.fda.gov

Compare with other makers

Updated March 18, 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.