Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Preat Corp with 11 device recalls and 4 510(k) clearances. The most recent is a device recall dated Jun 25, 2025: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 25, 2025 | NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662Class II · Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the c | Device recalls |
| Jun 24, 2025 | Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx OnlyClass II · Due to manufacturing error, digital analog rotational feature is 180 degrees off. | Device recalls |
| May 8, 2025 | Preat AbutmentsK243824 · NHA | 510(k) clearances |
| Apr 2, 2025 | Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with eClass II · Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the m | Device recalls |
| Jun 25, 2024 | Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-comClass II · Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually ins | Device recalls |
| Apr 10, 2024 | 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixtureClass II · Due to incorrect milled titanium abutment being packaged and labeled. | Device recalls |
| Feb 9, 2024 | Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967Class II · Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to h | Device recalls |
| Jul 18, 2023 | Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. DentalClass II · The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implan | Device recalls |
| Jul 18, 2023 | Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only. DentalClass II · The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implan | Device recalls |
| Oct 26, 2022 | Preat AbutmentsK220823 · NHA | 510(k) clearances |
| Mar 18, 2019 | Preat AbutmentsK183518 · NHA | 510(k) clearances |
| May 13, 1981 | ENDODONTIC POST SYSTEMSK810977 · ECG | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
