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Data / Medical devices / Finland / Delfin Technologies Ltd

Delfin Technologies Ltd: FDA-registered device maker in Kuopio Pohjois-Savo, Finland, 2 510(k) clearances

Delfin Technologies Ltd is registered with the FDA (registration 3004896338) in Kuopio Pohjois-Savo, Finland. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 27, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004896338
Address
Microkatu 1, Kuopio Pohjois-Savo, Finland, 70210
Owner or operator
Delfin Technologies Ltd (10053125)
Roles
Manufacturer
First device listed
November 2, 2016
Registered through
2026
Brand names listed
LymphScanner, MoistureMeterD

Devices it lists

DeviceProduct codeClassRoleSource
Monitor, Extracellular Fluid, Lymphedema, ExtremityOBH2Manufactureraccessdata.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
May 27, 2022K220557MoistureMeterD Compact, LymphScannerOBHSubstantially EquivalentDelfin Technologies, Ltd.accessdata.fda.gov
November 19, 2015K143310MoisturemeterDOBHSubstantially EquivalentDelfin Technologies, Ltd.accessdata.fda.gov

Compare with other makers

Updated May 27, 2022. 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.