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Data / Medical devices / Netherlands / Uv Smart Technologies B.V.

Uv Smart Technologies B.V.: FDA-registered device maker in Rijswijk Zuid-Holland, Netherlands, 1 510(k) clearance

Uv Smart Technologies B.V. is registered with the FDA (registration 3021233712) in Rijswijk Zuid-Holland, Netherlands. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 29, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021233712
Address
Patrijsweg 74, Rijswijk Zuid-Holland, Netherlands, 2289EX
Owner or operator
UV Smart Technologies B.V. (10083810)
Roles
Specification developer
First device listed
December 21, 2021
Registered through
2026
Brand names listed
UV Smart D25 (& Trolley), UV Smart D60

Devices it lists

DeviceProduct codeClassRoleSource
Disinfector, Medical DevicesMEC2Specification developeraccessdata.fda.gov
Ultraviolet Radiation Disinfection Chamber DeviceSCS2Specification 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
January 29, 2026K251354UV Smart D60SCSSubstantially EquivalentUV Smart Technologies B.V.accessdata.fda.gov

Compare with other makers

Updated January 29, 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.