Data / Medical devices / Italy / Italian Engineering SRL
Italian Engineering SRL: FDA-registered device maker in Bologna, Italy, 1 510(k) clearance
Italian Engineering SRL is registered with the FDA (registration 3012757453) in Bologna, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012757453
- Address
- Via Dell'elettricista 38, Bologna, Italy, 40138
- Owner or operator
- ITALIAN ENGINEERING SRL (10087501)
- Roles
- Manufacturer
- First device listed
- March 7, 2023
- Registered through
- 2026
- Brand names listed
- Attiva
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 9, 2023 | K220505 | ATTIVA | GEI | Substantially Equivalent | Italian Engineering S.R.L. | accessdata.fda.gov |
Compare with other makers
Updated February 9, 2023. 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.