510(k) K203360 ยท DZE Implant, Endosseous, Root-Form
EK Implants and Abutments System
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Jan 7, 2022 |
| Received | Nov 16, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203360
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.