LOCATOR Overdenture Implant SystemRecalls & reported problems across all models
Zest Anchors, LLC · 74 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one LOCATOR Overdenture Implant System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3,003
- Deaths reported
- 0
- Injuries reported
- 3,003
- Recalls
- 1
We found 74 models of LOCATOR Overdenture Implant System by Zest Anchors, LLC in the FDA's device registry (GUDID). Together they are named in 3,003 adverse event reports in the FDA's MAUDE database, received between May 15, 2019 and Sep 10, 2026 — classified as 3,003 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (1,703 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
LOCATOR Overdenture Implant System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 22, 2019Open, Classified
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
Z-2425-2020 · Root cause: Process control · names 5 of these models · Recall details · FDA record ↗
Most reported LOCATOR Overdenture Implant System problems
Device problems
- Failure to Osseointegrate1,703
- Loss of Osseointegration1,223
- Fracture93
- Adverse Event Without Identified Device or Use Problem1
- Contamination1
- Fitting Problem1
- Insufficient Device Problem Information1
Patient problems
- Failure of Implant1,461
- No Clinical Signs, Symptoms or Conditions1,118
- Inadequate Osseointegration152
- No Known Impact Or Consequence To Patient139
- Unspecified Infection63
- Pain46
- Inflammation45
- No Code Available34
LOCATOR Overdenture Implant System models
74 models, most reported first. Each model has its own page with its reports, recalls and device details.
- LOCATOR Overdenture Implant System 07450IMPLANT, ENDOSSEOUS, ROOT-FORM519 reports
- LOCATOR Overdenture Implant System 07460IMPLANT, ENDOSSEOUS, ROOT-FORM438 reports
- LOCATOR Overdenture Implant System 07461IMPLANT, ENDOSSEOUS, ROOT-FORM359 reports
- LOCATOR Overdenture Implant System 07451IMPLANT, ENDOSSEOUS, ROOT-FORM1 recall272 reports
- LOCATOR Overdenture Implant System 07465IMPLANT, ENDOSSEOUS, ROOT-FORM1 recall239 reports
- LOCATOR Overdenture Implant System 07455IMPLANT, ENDOSSEOUS, ROOT-FORM280 reports
- LOCATOR Overdenture Implant System 07466IMPLANT, ENDOSSEOUS, ROOT-FORM191 reports
- LOCATOR Overdenture Implant System 07456IMPLANT, ENDOSSEOUS, ROOT-FORM1 recall126 reports
- LOCATOR Overdenture Implant System 07462IMPLANT, ENDOSSEOUS, ROOT-FORM124 reports
- LOCATOR Overdenture Implant System 07467IMPLANT, ENDOSSEOUS, ROOT-FORM1 recall34 reports
- LOCATOR Overdenture Implant System 07452IMPLANT, ENDOSSEOUS, ROOT-FORM61 reports
- LOCATOR Overdenture Implant System 07476IMPLANT, ENDOSSEOUS, ROOT-FORM1 recall8 reports
- LOCATOR Overdenture Implant System 07470IMPLANT, ENDOSSEOUS, ROOT-FORM32 reports
- LOCATOR Overdenture Implant System 07457IMPLANT, ENDOSSEOUS, ROOT-FORM20 reports
- LOCATOR Overdenture Implant System 07440IMPLANT, ENDOSSEOUS, ROOT-FORM20 reports
- LOCATOR Overdenture Implant System 07441IMPLANT, ENDOSSEOUS, ROOT-FORM18 reports
- LOCATOR Overdenture Implant System 07502-02IMPLANT, ENDOSSEOUS, ROOT-FORM17 reports
- LOCATOR Overdenture Implant System 07444IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- LOCATOR Overdenture Implant System 07503-02IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- LOCATOR Overdenture Implant System 07443IMPLANT, ENDOSSEOUS, ROOT-FORM14 reports
- LOCATOR Overdenture Implant System 07381IMPLANT, ENDOSSEOUS, ROOT-FORM12 reports
- LOCATOR Overdenture Implant System 07507-03IMPLANT, ENDOSSEOUS, ROOT-FORM11 reports
- LOCATOR Overdenture Implant System 07506-03IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- LOCATOR Overdenture Implant System 07510-02IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- LOCATOR Overdenture Implant System 07386IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- LOCATOR Overdenture Implant System 07511-03IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- LOCATOR Overdenture Implant System 07509-02IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- LOCATOR Overdenture Implant System 07471IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- LOCATOR Overdenture Implant System 07501-02IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- LOCATOR Overdenture Implant System 07501-03IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- LOCATOR Overdenture Implant System 07502-03IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- LOCATOR Overdenture Implant System 07510-03IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- LOCATOR Overdenture Implant System 07503-03IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- LOCATOR Overdenture Implant System 07472IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- LOCATOR Overdenture Implant System 07511-04IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- LOCATOR Overdenture Implant System 07515-04IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- LOCATOR Overdenture Implant System 07475IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- LOCATOR Overdenture Implant System 07504-03IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- LOCATOR Overdenture Implant System 07507-04IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- LOCATOR Overdenture Implant System 07387IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07433IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07503-04IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07504-02IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07506-04IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07508-03IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- LOCATOR Overdenture Implant System 07477IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07435IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07501-04IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07502-05IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07502IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07503IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07506-02IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07509-04IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07510-04IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07511-02IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07512-02IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07512IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07513-02IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07514-03IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07515-02IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07515-03IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07516-04IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- LOCATOR Overdenture Implant System 07382IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07436IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07502-04IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07504-04IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07505-03IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07506-05IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07506IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07508-02IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07511-05IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07513-04IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07513IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- LOCATOR Overdenture Implant System 07514IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
Recent LOCATOR Overdenture Implant System adverse event reports
The 15 most recent reports across all models, 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 50703387 ↗InjurySep 10, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50703261 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50702457 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50702120 ↗InjurySep 9, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701593 ↗InjuryAug 25, 2026Failure to Osseointegrate
NON- INTEGRATION.PT CAME INTO OFFICE STATED IMPLANT SHOWING THROUGH THE GUM, X-RAY SHOWED NOT INTEGRATED. DR. REMOVED THE IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50440571 ↗InjuryAug 25, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50440570 ↗InjuryAug 25, 2026Failure to Osseointegrate
No information was provided by the account. Distributor states customer lost the implant. No product will be returned.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50440568 ↗InjuryAug 25, 2026Failure to Osseointegrate
No information was provided by the account. Distributor states customer lost the implant. No product will be returned.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50440567 ↗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 ↗InjuryJul 27, 2026Failure to Osseointegrate
NON INTEGRATION.patient walked into the office with the implant in their hand, his body rejected the implant, and there was no integration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047734 ↗InjuryJul 27, 2026Failure to Osseointegrate
NON INTEGRATION REPORTED NO OTHER INFORMATION REPORTED. ACCOUNT REPORTED THAT THERE WAS NO INJURY OR SURGICAL INTERVENTION REPORT FOR THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047733 ↗InjuryJul 27, 2026Failure to Osseointegrate
The Implant came out of the patients mouth together with the prosthesis. NON- INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047732 ↗InjuryJul 27, 2026Failure to Osseointegrate
Loss of integration and no other information was provided. ACCOUNT REPORTED THAT THERE WAS NO PATIENT INJURY OR SURGICAL INTERVENTION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047731 ↗InjuryJul 27, 2026Failure to Osseointegrate
IMPLANT FAILED TO INTEGRATE; NON-INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047730 ↗
Other Zest Anchors, LLC products
All Zest Anchors, LLC devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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