510(k) K172100 ยท DZE Implant, Endosseous, Root-Form
URIS OMNI System
| Applicant | Truabutment, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, May 4, 2018 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172100
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.