510(k) K240240 · NHA Abutment, Implant, Dental, Endosseous
Inclusive® Titanium Abutments compatible with: Keystone® Dental PrimaConnex®, Neodent® GM, Straumann® BLX, Implant Direct® Legacy®, Implant Direct® InterActive®, Implant Direct® RePlant® Implant Systems
| Applicant | Prismatik Dentalcraft, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jul 12, 2024 |
| Received | Jan 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240240
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.