510(k) K210828 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
DIOnavi-Denture02
| Applicant | Dio Corporation, Busan, KR |
| Decision | Substantially Equivalent, Mar 23, 2021 |
| Received | Mar 19, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210828
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.