Data / Medical devices / Post, Root Canal / Italy
FDA-registered makers of Post, Root Canal in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Post, Root Canal (product code ELR). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Post, Root Canal
- Product code
- ELR
- Country
- Italy
Makers of Post, Root Canal in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Kerr Italia, S.r.l. | SCAFATI Salerno, Italy | Manufacturer | 1 | November 9, 1998 | 0 | 0 | 0 | api.fda.gov |
| Bioloren SRL | SARONNO Varese, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micerium S.P.A. | AVEGNO Genova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Overfibers S.R.L | IMOLA Bologna, Italy | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rhein 83 SRL | BOLOGNA Emilia-Romagna, Italy | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.