LOCATOR Overdenture Implant System 07441Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.4mmD x 12mmL, 3mm Cuff · Class 2 · Implant
All models of LOCATOR Overdenture Implant System (74)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 18
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 00840481129711), received between Jun 30, 2022 and Sep 9, 2026 — classified as 18 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (15 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate15
- Loss of Osseointegration3
Patient problems
- No Clinical Signs, Symptoms or Conditions16
- Failure of Implant2
- Unspecified Infection1
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
InjurySep 9, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701593 ↗InjuryMar 3, 2026Failure to Osseointegrate
NON-INTEGRATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24499284 ↗InjuryMar 3, 2026Failure to Osseointegrate
NON-INTEGRATION AND INFECTION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24499283 ↗InjuryNov 14, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 16, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23069543 ↗InjuryMay 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PER CUSTOMER, IMPLANT FAILED TO TAKE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20865196 ↗InjuryFeb 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 23, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 23, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 23, 2023Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED. THE IMPLANT BECAME LOOSE AND WAS REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16304398 ↗InjuryOct 26, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15676674 ↗InjuryOct 26, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15676598 ↗InjuryOct 21, 2022Failure to Osseointegrate; Failure to Osseointegrate
FAILED IMPLANTS. NON-INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15653936 ↗InjuryOct 21, 2022Failure to Osseointegrate; Failure to Osseointegrate
FAILED IMPLANTS. NON-INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15653908 ↗InjuryJul 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. IMPLANTS FAILED TO INTEGRATE. PATIENT HAVE AN INFECTION.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 15086366 ↗InjuryJun 30, 2022Failure to Osseointegrate; Failure to Osseointegrate
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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