510(k) K122300 ยท DZE Implant, Endosseous, Root-Form
T3 DENTAL IMPLANT
| Applicant | Biomet 3i, Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Jan 30, 2013 |
| Received | Jul 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122300
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 10, 2015 | Biomet 3i, LLC 3i T3 Non-Platform Switched Tapered Implant Rx Only; 3.25 x 8.5 - 15.0 mm
Dental Implants. Terminated |
DZE | None listed |
| Aug 13, 2013 | Biomet 3i, LLC Biomet 3i Dental Implant, Parallel Walled 6mm (D) x 10mm (L) Terminated |
DZE | None listed |
| Aug 13, 2013 | Biomet 3i, LLC Biomet 3i Dental Implant, Non-Platform Switched Parallel Walled Implant 5mm (D) x 13mm (L) Terminated |
DZE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.