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Preat Implant ProstheticsRecalls & reported problems across all models

Preat Corporation · 13 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

6 open recalls name at least one Preat Implant Prosthetics model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
6

We found 13 models of Preat Implant Prosthetics by Preat Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

6 FDA recall records name at least one of these models by its device identifier, 6 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Preat Implant Prosthetics recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Jun 25, 2024Class IIOpen, Classified

    Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.

    Z-2687-2024 · Root cause: Process control · names 8 of these models · Recall details · FDA record ↗

  2. Apr 10, 2024Class IIOpen, Classified

    Due to incorrect milled titanium abutment being packaged and labeled.

    Z-2318-2024 · Root cause: Process control · Recall details · FDA record ↗

  3. Jul 18, 2023Class IIOpen, Classified

    The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

    Z-0154-2024 · Root cause: Process change control · Recall details · FDA record ↗

  4. Jul 18, 2023Class IIOpen, Classified

    The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

    Z-0153-2024 · Root cause: Process change control · Recall details · FDA record ↗

  5. Jul 18, 2023Class IIOpen, Classified

    The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

    Z-0152-2024 · Root cause: Process change control · Recall details · FDA record ↗

  6. Feb 21, 2023Class IIOpen, Classified

    Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture, which could result in the abutment/screw/crown being ingested by the patient.

    Z-1285-2023 · Root cause: Process design · Recall details · FDA record ↗

Preat Implant Prosthetics models

13 models, most reported first. Each model has its own page with its reports, recalls and device details.

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page