LOCATOR Overdenture Implant System 07506-03Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.9mmD x 10mmL, 3mm Cuff · Class 2 · Implant
All models of LOCATOR Overdenture Implant System (74)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00840481131028), received between Jul 20, 2022 and Jun 18, 2026 — classified as 10 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (9 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 Osseointegrate9
- Loss of Osseointegration1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
- Failure of Implant2
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryJun 18, 2026Failure to Osseointegrate
InjuryFeb 3, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 29, 2024Failure to Osseointegrate; Failure to Osseointegrate
INFECTION REPORTED FOR 3 IMPLANTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19202907 ↗InjuryMar 4, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 4, 2023Loss of Osseointegration; Loss of Osseointegration
STRIPPED SCREW. ABUTMENT DID NOT SEAT IN. DOCTOR. TRIED NEW ABUTMENT BUT STILL DID NOT TORQUING DOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18257724 ↗InjuryJun 12, 2023Failure to Osseointegrate; Failure to Osseointegrate
THE THREADS STRIPPED. NO OTHER INFORMATION WAS PROVIDED. FAILED INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17107380 ↗InjuryFeb 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16304646 ↗InjuryFeb 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16304395 ↗InjuryJul 20, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 20, 2022Failure to Osseointegrate; Failure to Osseointegrate
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- 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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