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Data / Medical devices / United Kingdom / Vascular Flow Technologies Ltd

Vascular Flow Technologies Ltd: FDA-registered device maker in Dundee Dundee City, United Kingdom, 1 510(k) clearance

Vascular Flow Technologies Ltd is registered with the FDA (registration 3007676031) in Dundee Dundee City, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 20, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007676031
Address
Michelin Scotland Innovation Parc Fulhame Building, Baldovie Rd, Dundee Dundee City, United Kingdom, DD4 8UQ
Owner or operator
Vascular Flow Technologies Limited (10029085)
Roles
Specification developer
First device listed
December 18, 2025
Registered through
2026
Brand names listed
Spiral Laminar FlowTM Vascular Arteriovenous Graft (AV0645)

Devices it lists

DeviceProduct codeClassRoleSource
Prosthesis, Vascular Graft, Of 6mm And Greater DiameterDSY2Specification developeraccessdata.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
October 20, 2025K252277Spiral Laminar Flow™ Vascular Arteriovenous Graft (AV0645)DSYSubstantially EquivalentVascular Flow Technologies Limitedaccessdata.fda.gov

Compare with other makers

Updated October 20, 2025. 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.