Data / Medical devices / Italy / Ceracarta SPA
Ceracarta SPA: FDA-registered device maker in Forli, Italy, 1 510(k) clearance
Ceracarta SPA is registered with the FDA (registration 3008506949) in Forli, Italy. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 15, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008506949
- Address
- Secondo Casadei,14, Forli, Italy, 47122
- Owner or operator
- CERACARTA SPA (10033758)
- Roles
- Manufacturer
- First device listed
- September 28, 2010
- Registered through
- 2026
- Brand names listed
- ECO SUPERGEL, ECO SUPERGEL CLEAR, RECORDING PAPER AND RECORDING CHART PAPER
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Recorder, Paper Chart | DSF | 1 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 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 |
|---|---|---|---|---|---|---|
| September 15, 2010 | K101429 | ECO SUPERGEL | IYO | Substantially Equivalent | Ceracarta Spa | accessdata.fda.gov |
Compare with other makers
Updated September 15, 2010. 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.