LOCATOR Overdenture Implant System 07387Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.9mmD x 12mmL · Class 2 · Implant
All models of LOCATOR Overdenture Implant System (74)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00840481129650), received between Jan 19, 2022 and Jan 19, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (3 reports).
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
- Failure to Osseointegrate3
Patient problems
- Failure of Implant3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 19, 2022Failure to Osseointegrate; Failure to Osseointegrate
DR STATES THERE WAS NO PRIMARY STABILITY WHEN HE WENT TO PLACE THE IMPLANT. NON-INTEGRATION.
Patient problems: Failure of Implant
MAUDE report 13289071 ↗InjuryJan 19, 2022Failure to Osseointegrate; Failure to Osseointegrate
DR STATES THERE WAS NO PRIMARY STABILITY WHEN HE WENT TO PLACE THE IMPLANT. NON-INTEGRATION.
Patient problems: Failure of Implant
MAUDE report 13289066 ↗InjuryJan 19, 2022Failure to Osseointegrate; Failure to Osseointegrate
DR STATES THERE WAS NO PRIMARY STABILITY WHEN HE WENT TO PLACE THE IMPLANT. NON-INTEGRATION.
Patient problems: Failure of Implant
MAUDE report 13289065 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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