510(k) K182422 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
Lucitone Denture Base Materials
| Applicant | Dentsply Sirona, York PA, US |
| Decision | Substantially Equivalent, Dec 18, 2018 |
| Received | Sep 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182422
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.