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Data / Medical devices / Spain / Toskani

Toskani: FDA-registered device maker in Barcelona, Spain, 1 510(k) clearance

Toskani is registered with the FDA (registration 3010290186) in Barcelona, Spain. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 7, 2018. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3010290186
Address
Ptje. Ciutadans 4, Barcelona, Spain, 08005
Owner or operator
Toskani (10090033)
Roles
Complaint file establishment, Exporter to the US, Foreign private label distributor, Manufacturer, Repackager or relabeler
First device listed
February 6, 2024
Registered through
2027
Brand names listed
MTDerm, TKN MesojectGun, TOSKANIMED

Devices it lists

DeviceProduct codeClassRoleSource
Massager, Therapeutic, ElectricISA1Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Powered Microneedle DeviceQAI2Exporter to the USaccessdata.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
September 7, 2018K180778Exceed Microneedling DeviceQAISubstantially EquivalentMt. Derm GmbHaccessdata.fda.gov

Compare with other makers

Updated September 7, 2018. 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.