LOCATOR Overdenture Implant System 07502Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.5mmD x 10mmL · 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
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840481130854), received between Nov 8, 2021 and Mar 4, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (2 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 Osseointegrate2
Patient problems
- Failure of Implant2
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 4, 2022Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION REPORTED. 4 IMPLANTS PLACE (B)(6) 2021 IN LOWER JAW 3 OF THE 4 DID NOT INTEGRATE. PATIENT IS UNDER PHYSICIAN CARE FOR BONE PROBLEM.
Patient problems: Failure of Implant
MAUDE report 13669692 ↗InjuryNov 8, 2021Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. 4 LODI IMPLANTS WERE PLACED (B)(6) 2021, AFTER EXTRACTORS + ALVEB. SWELLING + PAIN REPORTED BY PATIENT (B)(6) 2021. IMPLANT REMOVAL (B)(6) 2021- LOOSE.
Patient problems: Failure of Implant; Pain; Swelling/ Edema
MAUDE report 12775201 ↗
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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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