LOCATOR Overdenture Implant System 07466Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.9mmD x 12mmL, 4mm 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 LOCATOR overdenture implant is a dental implant placed in the jawbone to support a denture. Its 191 reports mostly describe implants that failed to bond with the bone, or lost that bond later, and some implants that had to be removed. All 191 are listed as injuries, and there are no deaths. No recalls name this device. Reports fell from 19 in the year before to 6 in the latest year.
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
- 191
- Deaths reported
- 0
- Injuries reported
- 191
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 191 adverse event reports that list this exact device (DI 00840481101588), received between May 28, 2019 and Sep 10, 2026 — classified as 191 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (104 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 Osseointegrate104
- Loss of Osseointegration84
- Fracture2
- Contamination1
Patient problems
- Failure of Implant97
- No Clinical Signs, Symptoms or Conditions74
- No Known Impact Or Consequence To Patient10
- Inadequate Osseointegration8
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Hepatitis2
- No Code Available2
- Pain1
Recent adverse event reports
The 25 most recent of 191 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 50703387 ↗InjuryMay 7, 2026Failure to Osseointegrate
NON-INTEGRATION NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25117074 ↗InjuryApr 2, 2026Loss of Osseointegration
LOSS OF INTEGRATION AND FAILED TO INTEGRATE AND WERE REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24767494 ↗InjuryDec 22, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23872879 ↗InjuryNov 14, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23556961 ↗InjuryNov 3, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 8, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23251104 ↗InjuryMay 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 15, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 15, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 17, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21861640 ↗InjuryApr 10, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21821136 ↗InjuryApr 10, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21821134 ↗InjuryApr 4, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21774404 ↗InjuryMar 26, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21701491 ↗InjuryFeb 25, 2025Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. IT WAS REPORTED THAT THE IMPLANTS FAILED TO INTEGRATE AND WERE REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21460238 ↗InjuryFeb 25, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION. DOCTOR REPORTED LOSS OF INTEGRATION WITH EDEMA AND PAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21459121 ↗InjuryFeb 18, 2025Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. NO INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21402539 ↗InjuryJan 31, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21283905 ↗InjuryJan 30, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21276693 ↗InjuryJan 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. NO PRIMARY STABILITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21267668 ↗InjuryJan 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 29, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21266040 ↗InjuryJan 27, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS IF INTEGRATION AND NO OTHER DETAIL INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21245885 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
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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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