Atlantis 36462Recalls & reported problems
Dentsply Ih, Inc. · ATLANTIS Hybrid Ti AM · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07392532182518), received between Jun 5, 2025 and Jun 5, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Separation Failure” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Separation Failure1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 5, 2025Separation Failure; Separation Failure
IN THIS EVENT IT IS REPORTED THAT A S ATLANTIS ABUTMENT TI - ABUTMENT SCREW BROKE INSIDE THE IMPLANT. PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. ATLANTIS SUPERSTRUCTURE NEED RETRIEVAL TOOLS
Patient problems: Failure of Implant
MAUDE report 22148777 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.