Data / Medical devices / Italy / Spazzolificio Piave SPA
Spazzolificio Piave SPA: FDA-registered device maker in ONARA DI TOMBOLO Padova, Italy, 1 510(k) clearance
Spazzolificio Piave SPA is registered with the FDA (registration 1000252128) in ONARA DI TOMBOLO Padova, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 3, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000252128
- Address
- Via A Palladio,5, ONARA DI TOMBOLO Padova, Italy, 35019
- Owner or operator
- SPAZZOLIFICIO PIAVE S.P.A. (9022949)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- October 20, 1995
- Registered through
- 2026
- Brand names listed
- Co Bigelow, Marvis, Piave, Silver Care
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Toothbrush, Manual | EFW | 1 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| October 3, 2011 | K102871 | SILVER CARE ANITBACTERIAL TOOTHBRUSH | EFW | Substantially Equivalent | Piave Spazzolificio S.P.A. | accessdata.fda.gov |
Compare with other makers
Updated October 3, 2011. 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.