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Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / Italy

FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in Italy: 7 establishments

7 establishments in Italy are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Shoulder Prosthesis, Reverse Configuration
Product code
PHX
Country
Italy

Makers of Shoulder Prosthesis, Reverse Configuration in Italy

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Limacorporate S.p.A.Villanova di San Daniele Udine, ItalyManufacturer11January 22, 2026010api.fda.gov
Eddi Bressan S.R.L.CORMONS Gorizia, ItalyContract manufacturer0000api.fda.gov
HPF S.R.L.Forgaria nel Friuli Friuli Venezia Giulia, ItalyContract manufacturer0000api.fda.gov
Limacorporate S.p.A.Calatafimi Segesta (TP) Sicilia, ItalyContract manufacturer, Manufacturer0000api.fda.gov
Oeb S.R.L.Camposanto Modena, ItalyContract manufacturer0000api.fda.gov
Sti Lualdi S.R.L.Casiacco Pordenone, ItalyContract manufacturer0000api.fda.gov
Valtecne SPABerbenno di Valtellina Sondrio, ItalyContract manufacturer0000api.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.