Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Italy
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Italy: 10 establishments
10 establishments in Italy are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 9 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
- Electrosurgical, Cutting & Coagulation & Accessories
- Product code
- GEI
- Country
- Italy
Makers of Electrosurgical, Cutting & Coagulation & Accessories in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| H.S. Hospital Service S.P.A. | Rome Roma, Italy | Manufacturer | 3 | February 9, 2024 | 0 | 0 | 0 | api.fda.gov |
| Triworks Group S.R.L. | Palata Campobasso, Italy | Manufacturer | 2 | July 7, 2022 | 0 | 0 | 0 | api.fda.gov |
| Axon SRL | Pompei Napoli, Italy | Manufacturer | 1 | August 30, 2023 | 0 | 0 | 0 | api.fda.gov |
| Bios S.R.L. | VIMODRONE Milano, Italy | Manufacturer | 1 | August 11, 2023 | 0 | 0 | 0 | api.fda.gov |
| Fiab SPA | Vicchio Firenze, Italy | Manufacturer | 1 | June 21, 2010 | 0 | 0 | 0 | api.fda.gov |
| GMV S.R.L. | roma, Italy | Manufacturer | 1 | March 22, 2022 | 0 | 0 | 0 | api.fda.gov |
| Italian Engineering SRL | Bologna, Italy | Manufacturer | 1 | February 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| Led SPA | Aprilia Latina, Italy | Manufacturer | 1 | October 5, 2022 | 0 | 0 | 0 | api.fda.gov |
| Telea Electronic Engineering S.R.L. | Sandrigo Vicenza, Italy | Manufacturer | 1 | January 31, 2014 | 0 | 0 | 0 | api.fda.gov |
| El.en. Electronic Engineering SPA | CALENZANO Firenze, 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.