510(k) K233389 ยท NHA Abutment, Implant, Dental, Endosseous
EK Digital Abutments
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, May 29, 2024 |
| Received | Oct 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233389
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.