Data / Medical devices / Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use / Italy
FDA-registered makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Italy: 10 establishments
10 establishments in Italy are registered with the FDA to make Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use (product code LXG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- Product code
- LXG
- Country
- Italy
Makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| APTACA S.p.A. | Canelli Asti, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biosigma SPA | Cantarana di Cona (VE) Veneto, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copan Italia | BRESCIA Lombardy, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copan WASP | Brescia Lombardy, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| F.L. Medical S.R.L. Unipersonale | Torreglia Padova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Human Brain Wave SRL | Torino, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kartell SPA | NOVIGLIO Milano, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDESY srl | MANIAGO Pordenone, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Milestone S.P.A. | Sorisole Bergamo, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ROLL Srl | Piove di Sacco Padova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.