510(k) K251938 ยท DZE Implant, Endosseous, Root-Form
GEN5 and GEN5+ Dental Implant System
| Applicant | Paragon Implant Mfg., LLC, Calabasas CA, US |
| Decision | Substantially Equivalent, Oct 30, 2025 |
| Received | Jun 24, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251938
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.