LOCATOR Overdenture Implant System 07450Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.4mmD x 10mmL, 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 dental implant has 520 adverse event reports, with no deaths and 520 injuries. Most reports describe the implant failing to fuse with the jawbone, and a few describe fractures or implants coming out with the denture. No recalls name this device. Reports fell to 15 in the last 12 months from 37 in the year before.
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
- 519
- Deaths reported
- 0
- Injuries reported
- 519
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 519 adverse event reports that list this exact device (DI 00840481101489), received between May 15, 2019 and Aug 25, 2026 — classified as 519 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (268 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 Osseointegrate268
- Loss of Osseointegration227
- Fracture28
- Insufficient Device Problem Information1
Patient problems
- Failure of Implant276
- No Clinical Signs, Symptoms or Conditions158
- No Known Impact Or Consequence To Patient29
- Inadequate Osseointegration28
- Pain13
- Discomfort6
- Inflammation6
- Implant Pain5
Recent adverse event reports
The 25 most recent of 519 reports, in the reporter's own words as published by the FDA.
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 ↗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 ↗InjuryJul 27, 2026Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047729 ↗InjuryJul 27, 2026Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50047726 ↗InjuryApr 21, 2026Failure to Osseointegrate
NO HAZARD OR ANY OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24947832 ↗InjuryApr 2, 2026Loss of Osseointegration
LOSS OF INTEGRATION REPORTED. NO OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24767519 ↗InjuryApr 2, 2026Loss of Osseointegration
LOSS OF INTEGRATION REPORTED. NO OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24767516 ↗InjuryMar 12, 2026Loss of Osseointegration
LOSS OF INTEGRATION AND NO OTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24581166 ↗InjuryMar 3, 2026Fracture
FRACTURED IMPLANT AT SCREW REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24499287 ↗InjuryNov 14, 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 23251103 ↗InjurySep 2, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 29, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22928130 ↗InjuryAug 29, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22928126 ↗InjuryJul 1, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 16, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 16, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 16, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 16, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22215584 ↗InjuryJun 16, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22215152 ↗InjuryJun 11, 2025Failure 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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