LOCATOR Overdenture Implant System 07462Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.9mmD 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
Quick summary
This Zest Anchors LOCATOR overdenture implant has 123 adverse event reports, with no deaths and 123 injuries. Reports most often describe implants that did not bond with the jawbone or lost that bond over time, leading to their removal, and some mention infection or inflammation. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 124
- Deaths reported
- 0
- Injuries reported
- 124
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 124 adverse event reports that list this exact device (DI 00840481101564), received between May 28, 2019 and Sep 10, 2026 — classified as 124 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (64 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 Osseointegrate64
- Loss of Osseointegration59
- Fracture1
Patient problems
- Failure of Implant59
- No Clinical Signs, Symptoms or Conditions23
- Inflammation15
- No Known Impact Or Consequence To Patient12
- Inadequate Osseointegration11
- Insufficient Information3
- Implant Pain2
- Unspecified Infection2
Recent adverse event reports
The 25 most recent of 124 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50703261 ↗InjuryAug 11, 2026Loss of Osseointegration
LOSS OF INTEGRATION.THE IMPLANT AT TOOTH SITE #42 LOST INTEGRATION AND WAS REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50201444 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF INTEGRATION REPORTED AND INFECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24217986 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF INTEGRATION REPORTED AND INFECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24217982 ↗InjuryAug 14, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION. IT WAS REPORTED THAT THE IMPLANT LOST INTEGRATION AND WAS REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22806455 ↗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 21404205 ↗InjuryJan 31, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 16, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 16, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 6, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18852715 ↗InjuryJan 30, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18606675 ↗InjuryJan 22, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 22, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 20, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON- INTEGRATION WAS REPORTED AND DENTAL IMPLANT LOCATED IN DENTAL POSITION UMNER #43 FAILED DUE TO PERI-IMPLANTITIS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18368006 ↗InjuryNov 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 4, 2023Loss of Osseointegration; Loss of Osseointegration
NON-INTEGRATION AFTER 2 WEEKS IN PAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17871442 ↗InjurySep 27, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. FAILED PRIMARY STABILITY AND INFECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17825726 ↗InjuryAug 18, 2023Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17576662 ↗InjuryJul 25, 2023Loss of Osseointegration; Loss of Osseointegration
LOOS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17393461 ↗InjuryOct 29, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEO-INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15695381 ↗InjuryOct 24, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15663496 ↗InjuryOct 24, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15663453 ↗InjuryOct 5, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 20, 2022Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT THE IMPLANT AT POSITION #25 FAILED TO INTEGRATE AND WAS REMOVED. LOSS OF INTEGRATION.
Patient problems: Implant Pain
MAUDE report 15459323 ↗
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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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