510(k) K181037 ยท NHA Abutment, Implant, Dental, Endosseous
DIO CAD/CAM Abutment
| Applicant | Dio Corporation, Busan, KR |
| Decision | Substantially Equivalent, Dec 21, 2018 |
| Received | Apr 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181037
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.