OSSEOTITE® OSS513Recalls & reported problems
ZimVie US Corp LLC · OSSEOTITE® IMPLANT 5 X 13MM · Class 2 · Implant
All models of OSSEOTITE (73)
Data updated Oct 16, 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 00844868013273), received between Mar 23, 2020 and Jan 7, 2021 — classified as 2 injuries.
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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Edema1
- No Code Available1
- No Information1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 30 LACKED PRIMARY STABILITY WHEN PLACING AND IT WAS REMOVED. NO OTHER IMPLANT WAS USED TO COMPLETE THE PROCEDURE. SYMPTOMS AS A RESULT OF THE EVENT: EDEMA
Patient problems: Edema; No Information
MAUDE report 11133703 ↗InjuryMar 23, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT OSS513 PLACED IN DENTAL SITE 30 WAS REMOVED DUE TO PERI-IMPLANTITIS. NO OTHER IMPLANT WAS PLACED IN THE SAME PROCEDURE.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 9864476 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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