LOCATOR Overdenture Implant System 07507-03Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.9mmD x 12mmL, 3mm 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
- 11
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00840481131073), received between Nov 15, 2022 and Feb 18, 2025 — classified as 11 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (5 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 Osseointegrate5
- Fracture5
- Loss of Osseointegration1
Patient problems
- No Clinical Signs, Symptoms or Conditions11
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
InjuryFeb 18, 2025Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. IMPLANTS DID NOT INTEGRATE INTO THE BONE AND WERE REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21406627 ↗InjuryJan 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
CUSTOMER STATES THAT THERE WAS LACK OF INTEGRATION..NON INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21257464 ↗InjuryApr 29, 2024Failure to Osseointegrate; Failure to Osseointegrate
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 19202921 ↗InjuryMar 25, 2024Fracture; Fracture
NON- INTEGRATION. IMPLANTS FAILED INSTANTLY DURING SURGERY PLACEMENT. AND FRACTURE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18969068 ↗InjuryMar 25, 2024Fracture; Fracture
NON- INTEGRATION. IMPLANTS FAILED INSTANTLY DURING SURGERY PLACEMENT. AND FRACTURE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18969067 ↗InjuryMar 25, 2024Fracture; Fracture
NON- INTEGRATION. IMPLANTS FAILED INSTANTLY DURING SURGERY PLACEMENT. AND FRACTURE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18969066 ↗InjuryMar 15, 2024Fracture; Fracture
NON- INTEGRATION. IMPLANTS FAILED INSTANTLY DURING SURGERY PLACEMENT. AND FRACTURE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18918040 ↗InjuryMar 15, 2024Fracture; Fracture
NON- INTEGRATION. IMPLANTS FAILED INSTANTLY DURING SURGERY PLACEMENT. AND FRACTURE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18918039 ↗InjuryMay 3, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 15, 2022Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15798819 ↗
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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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