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RePlant® Implant Analog 6043-06DRecalls & reported problems

Implant Direct Sybron Manufacturing LLC · Class 1 · Implant

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841307123903), received between Apr 11, 2019 and Apr 11, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Misassembled During Manufacturing /Shipping” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Misassembled During Manufacturing /Shipping1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 11, 2019Device Misassembled During Manufacturing /Shipping; Device Misassembled During Manufacturing /Shipping

    PER COMPLAINT (B)(4), IT WAS DISCOVERED THAT THERE WAS AN ISSUE OF ORIENTATION ON A 3D PRINTED MODEL OF A DENTAL IMPLANT ANALOG. THE LOBES AND FLATS OF THE PART WERE NOT ALIGNED CORRECTLY.

    Patient problems: No Patient Involvement

    MAUDE report 8506769 ↗

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Sources and updates

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