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Data / Medical devices / Implant, Endosseous, Root-Form / Italy

FDA-registered makers of Implant, Endosseous, Root-Form in Italy: 5 establishments

5 establishments in Italy are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 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
Implant, Endosseous, Root-Form
Product code
DZE
Country
Italy

Makers of Implant, Endosseous, Root-Form in Italy

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
J Dental Care SRLModena, ItalyManufacturer5September 25, 2025000api.fda.gov
Sweden & Martina S.P.A.Due Carrare Padova, ItalyManufacturer3July 8, 2019000api.fda.gov
HDC S.R.L.THIENE Vicenza, ItalyManufacturer2October 18, 2007000api.fda.gov
Leone SPASesto Fiorentino Firenze, ItalyManufacturer1February 27, 2006000api.fda.gov
Rhein 83 SRLBOLOGNA Emilia-Romagna, ItalyComplaint file establishment, Manufacturer1April 21, 2004000api.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.