LOCATOR Overdenture Implant System 07503-02Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.5mmD x 12mmL, 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
- 15
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00840481130861), received between Sep 14, 2021 and Jan 29, 2026 — classified as 15 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (9 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.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate9
- Loss of Osseointegration5
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions14
- Failure of Implant1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
InjuryJan 29, 2026Failure to Osseointegrate
NON-INTEGRATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24217984 ↗InjuryDec 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
NON- INTEGRATION. LACK OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23872860 ↗InjuryFeb 3, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 20, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION REPORTED WITH NO FURTHER EVENT DETAILS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20989038 ↗InjuryJun 14, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19541535 ↗InjuryJun 14, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION. IMPLANT CAME OUT. NO OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19540713 ↗InjuryJun 14, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION. IMPLANT CAME OUT. NO OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19540677 ↗InjuryApr 29, 2024Loss of Osseointegration; Loss of Osseointegration
INFECTION REPORTED FOR 3 IMPLANTS. NO OTHER INFORMATION WAS PROVIDED IF IMPLANTS WERE REMOVED OR NOT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19202910 ↗InjuryDec 26, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 26, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PT. CAME IN IMPLANTS WERE MOBIL-FAILED IMPLANTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17939658 ↗InjuryOct 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PT. CAME IN IMPLANTS WERE MOBIL-FAILED IMPLANTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17939656 ↗InjuryOct 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PT. CAME IN IMPLANTS WERE MOBIL-FAILED IMPLANTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17939654 ↗InjuryAug 25, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 14, 2021Fracture; Fracture
(B)(6) FROM DR (B)(6) OFFICE SAID "THE TOP BROKE OFF OF THIS IMPLANT" AS DR (B)(6) WAS PLACING IT.
Patient problems: Failure of Implant
MAUDE report 12471184 ↗
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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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