Data / Medical devices / Italy / CANE' S.p.A.
CANE' S.p.A.: FDA-registered device maker in RIVOLI-CASCINE VICA Torino, Italy, 4 510(k) clearances
CANE' S.p.A. is registered with the FDA (registration 3003098013) in RIVOLI-CASCINE VICA Torino, Italy. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated May 12, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003098013
- Address
- Via Cuorgne, 42/a, RIVOLI-CASCINE VICA Torino, Italy, 10098
- Owner or operator
- CANE S.p.A. (9049153)
- Roles
- Manufacturer
- First device listed
- May 10, 2006
- Registered through
- 2026
- Brand names listed
- CRONO SUPER PID, Crono, Crono 30, Crono S-PID 50, Crono go, Cronobell cartridge holder, ONAPGO Pump
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Pump, Infusion | MRZ | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Infusion | FRN | 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 |
|---|---|---|---|---|---|---|
| May 12, 2009 | K091042 | CRONO S-PID 50 | FRN | Substantially Equivalent | Cane S.R.L. | accessdata.fda.gov |
| September 13, 2005 | K052219 | CRONO GO. | FRN | Substantially Equivalent | Cane S.R.L. | accessdata.fda.gov |
| September 13, 2005 | K052217 | CRONO SUPER PID | FRN | Substantially Equivalent | Cane S.R.L. | accessdata.fda.gov |
| July 8, 2004 | K041414 | CRONO AND CRONO, MODEL 30 | FRN | Substantially Equivalent | Cane S.R.L. | accessdata.fda.gov |
Compare with other makers
Updated May 12, 2009. 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.