LOCATOR Overdenture Implant System 07508-03Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.9mmD x 14mmL, 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
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00840481131127), received between Nov 18, 2021 and Nov 15, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (3 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.
Most reported problems
Device problems
- Failure to Osseointegrate3
Patient problems
- Failure of Implant2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 15, 2022Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED. FAILED LODI. IMPLANT WAS LOOSE AND DID NOT INTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15798845 ↗InjuryJun 17, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 18, 2021Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. WHILE DOCTOR. IS PLACING IMPLANT THE EXTERNAL HEX BRANDISHING OFF AND BECOMES SMOOTH SEATING AT 35 NCM WITH HANDPIECE AND TRYING TO FINISHING TORQUING AND WILL STRIP WITH MANUAL WRENCH.
Patient problems: Failure of Implant
MAUDE report 12839085 ↗
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- 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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