510(k) K240232 ยท DZE Implant, Endosseous, Root-Form
EK D3.3 and Ultra Wide Implants
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Sep 13, 2024 |
| Received | Jan 29, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240232
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.