LOCATOR Overdenture Implant System 07452Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 2.4mmD x 14mmL, 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 overdenture implant is a small root-form dental implant used to anchor a denture. The 61 reports mostly describe implants that fail to bond with the jawbone or later lose that bond, along with a few fractures and some cases of swelling or infection. There are no deaths; all 61 reports describe injuries. No recalls name this device.
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
- 61
- Deaths reported
- 0
- Injuries reported
- 61
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 61 adverse event reports that list this exact device (DI 00840481101502), received between Jul 5, 2019 and Dec 29, 2025 — classified as 61 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (33 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 Osseointegrate33
- Loss of Osseointegration25
- Fracture4
Patient problems
- Failure of Implant40
- No Clinical Signs, Symptoms or Conditions16
- Inadequate Osseointegration4
- Unspecified Infection3
- Osteolysis2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Inflammation1
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 61 reports, in the reporter's own words as published by the FDA.
InjuryDec 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 5, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 26, 2024Fracture; Loss of Osseointegration; Fracture; Loss of Osseointegration
LOSS OF INTEGRATION AND FRACTURED IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19193536 ↗InjuryApr 3, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 3, 2024Failure to Osseointegrate; Failure to Osseointegrate
NM NON- INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19038033 ↗InjuryApr 3, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 27, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. FAILED PRIMARY STABILITY AND INFECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17825610 ↗InjurySep 25, 2023Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17807242 ↗InjuryMay 12, 2023Fracture; Fracture
IMPLANT FRACTURED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16923968 ↗InjuryApr 4, 2023Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16674259 ↗InjuryMar 2, 2023Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16467918 ↗InjuryFeb 15, 2023Failure to Osseointegrate; Failure to Osseointegrate
NO OTHER INFORMATION WAS REPORTED BY THE ACCOUNT AND BLANK PRODUCT EXPERIENCE REPORT WAS SENT WITH PART NUMBER AND LOT NUMBER. NON-INTEGRATION HAS BEEN SELECTED FOR REPORTING PURPOSES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16382601 ↗InjurySep 16, 2022Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15439616 ↗InjuryJun 27, 2022Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT THE IMPLANT AT POSITION 15 FAILED TO INTEGRATE AND WAS REMOVED.
Patient problems: Failure of Implant
MAUDE report 14836007 ↗InjuryJun 27, 2022Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT THE IMPLANT AT POSITION 13 FAILED TO INTEGRATE AND WAS REMOVED.
Patient problems: Failure of Implant
MAUDE report 14834728 ↗InjuryMay 10, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 10, 2022Fracture; Fracture
InjuryMay 6, 2022Loss of Osseointegration; Loss of Osseointegration
DOCTOR REPORTED LOSS OF INTEGRATION WITH INFLAMMATION, SWELLING AND PAIN. LOSS OF INTEGRATION.
Patient problems: Failure of Implant; Inflammation; Pain; Swelling/ Edema
MAUDE report 14306079 ↗InjuryApr 12, 2022Loss of Osseointegration; Loss of Osseointegration
InjuryApr 12, 2022Loss of Osseointegration; Loss of Osseointegration
InjuryDec 31, 2021Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE 33 FAILED TO INTEGRATE DUE TO BONE LOSS AND INFECTION AND WAS REMOVED. PER INDICATED: NON INTEGRATED, BONE LOSS, INFECTION. ADDITIONAL APPOINTMENT REQUIRED: YES, TO PLACE A NEW IMPLANT. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Failure of Implant; Osteolysis; Unspecified Infection
MAUDE report 13125568 ↗InjuryDec 22, 2021Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PRIMARY STABILITY COULD NOT BE ACHIEVED.
Patient problems: Failure of Implant
MAUDE report 13064082 ↗
Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page