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Data / Medical devices / Italy / Delta International Service & Logistics S.R.L.

Delta International Service & Logistics S.R.L.: FDA-registered device maker in Roma, Italy, 1 510(k) clearance

Delta International Service & Logistics S.R.L. is registered with the FDA (registration 3012440948) in Roma, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 23, 2020. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3012440948
Address
Piazza Adriana 4, Roma, Italy, 00193
Owner or operator
Delta international Service & Logistics S.r.l. (10050207)
Roles
Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer
First device listed
April 26, 2021
Registered through
2026
Brand names listed
Scrambler Therapy® Technology ST-5A

Devices it lists

DeviceProduct codeClassRoleSource
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Exporter to the US, Foreign private label distributor, Manufacturer, Specification 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
December 23, 2020K201458Scrambler Therapy Technology (Model ST-5A)GZJSubstantially EquivalentDelta International Services & Logistics S.R.Laccessdata.fda.gov

Compare with other makers

Updated December 23, 2020. 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.