LOCATOR Overdenture Implant System 07501-02Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.5mmD x 8mmL, 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
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00840481130762), received between Oct 20, 2022 and Jan 14, 2025 — classified as 7 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (6 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 Osseointegrate6
- Loss of Osseointegration2
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryJan 14, 2025Failure to Osseointegrate; Loss of Osseointegration; Failure to Osseointegrate; Loss of Osseointegration
DR. (B)(6) REPORTED IMPLANT LOST INTEGRATION AND THE IMPLANT WAS REMOVED FULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21153438 ↗InjuryAug 26, 2024Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION AND NOT OTHER INFORMATION REPORTED BY THE ACCOUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20065430 ↗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 19202918 ↗InjuryApr 29, 2024Failure to Osseointegrate; Failure to Osseointegrate
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 19202914 ↗InjuryDec 21, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. ALL ON 4 SNAP ON DENTURE PLACED DAY OF SURGERY BUT DID NOT LOAD #29.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18373018 ↗InjuryApr 19, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. DR YOST CALLED IN (B)(6) 2023 THAT HIS LODI IMPLANTS DID NOT HAVE OSSEO-INTEGRATION ON ONE PT. DR PLACED 6 LODIS ON (B)(6) 2023, THEY STARTED FAILING 3 WEEKS LATER AND BY (B)(6) 2023 THEY WERE ALL OUT. DR DID NOT HAVE REFERENCE NUMBERS OR LOT NUMBERS. HE PROVIDED ME IMPLANT SPECS AND I AM INPUTTING MY EDUCATED GUESS ON REF AND LOT NUMBERS IN THE NOTES SECTION BELOW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16773190 ↗InjuryOct 20, 2022Failure to Osseointegrate; Failure to Osseointegrate
NON- INTEGRATION. IMPLANT FAILED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15642786 ↗
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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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