LOCATOR Overdenture Implant System 07508-02Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.9mmD x 14mmL, 2.5mm Cuff · 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
- 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 00840481131110), received between Dec 22, 2025 and Dec 22, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Fitting Problem” (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.
Reports received per month
Most reported problems
Device problems
- Fitting Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2025Fitting Problem; Fitting Problem
CUSTOMER STATES THAT THE IMPLANT WAS NOT TORQUING DOWN AND THEY ALSO COULD NOT GET THE IMPLANT OUT OF THE PATIENTS MOUTH SO THEY HAD TO DRILL IT OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23872873 ↗
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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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