510(k) K183518 ยท NHA Abutment, Implant, Dental, Endosseous
Preat Abutments
| Applicant | Preat Corporation, Grover Beach CA, US |
| Decision | Substantially Equivalent, Mar 18, 2019 |
| Received | Dec 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183518
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 3, 2025 | Preat Corp NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662 Open, Classified |
NHA | None listed |
| Jun 18, 2025 | Preat Corp Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F
Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch Open, Classified |
NHA | None listed |
| Mar 20, 2024 | Preat Corp Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 Open, Classified |
NHA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.