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Data / Medical devices / Syringe, Piston / Italy

FDA-registered makers of Syringe, Piston in Italy: 7 establishments

7 establishments in Italy are registered with the FDA to make Syringe, Piston (product code FMF). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Syringe, Piston
Product code
FMF
Country
Italy

Makers of Syringe, Piston in Italy

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aea SRLAngeli di Rosora Ancona, ItalyComplaint file establishment, Specification developer2December 17, 2020000api.fda.gov
Adria.med. SRLTocco Da Casauria Pescara, ItalyContract manufacturer, Contract sterilizer, Manufacturer1March 21, 2014000api.fda.gov
Artiglass SRLDue Carrare Padova, ItalyManufacturer1May 3, 2013000api.fda.gov
Pentaferte Italia S.R.L.CAMPLI Teramo, ItalyManufacturer1January 11, 2001000api.fda.gov
PIKDARE S.p.A.Casnate con Bernate Como, ItalyContract manufacturer, Contract sterilizer, Exporter to the US, Manufacturer1November 25, 2005000api.fda.gov
Delta Med SpAviadana Mantova, ItalyContract manufacturer0000api.fda.gov
Roncadelle Operations SRLCastel Mella Brescia, ItalyManufacturer0000api.fda.gov

Updated November 2, 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.