3i T3® BOST3210Recalls & reported problems
ZimVie US Corp LLC · 3i T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 10MM · Class 2 · Implant
Quick summary
This 3i T3 dental implant has 133 reports, many describing bone loss around the implant and infection, with some implants removed. The reports mention 130 injuries and no deaths, and 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
- 133
- Deaths reported
- 0
- Injuries reported
- 130
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 133 adverse event reports that list this exact device (DI 00844868028871), received between Feb 7, 2020 and Sep 17, 2026 — classified as 130 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Fracture” (10 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem121
- Fracture10
- Loss of Osseointegration2
- Detachment of Device or Device Component1
- Mechanical Problem1
- Separation Problem1
Patient problems
- Unspecified Infection71
- Osteolysis69
- Pain29
- Inflammation18
- No Clinical Signs, Symptoms or Conditions14
- No Code Available11
- Swelling/ Edema7
- No Information6
Recent adverse event reports
The 25 most recent of 133 reports, in the reporter's own words as published by the FDA.
InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem
It was reported that two implants were removed due to a bone loss. Tooth sites 22 and 27.Bone density type: I.
Patient problems: Osteolysis
MAUDE report 50799254 ↗InjuryApr 29, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #24 LOST INTEGRATION AND WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Osteolysis; Pain; Unspecified Infection
MAUDE report 25027590 ↗InjuryApr 15, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN IMPLANT AT TOOTH SITE # 26 WAS REMOVED DUE TO A BONE LOSS.
Patient problems: Osteolysis
MAUDE report 24887792 ↗InjuryApr 7, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #12 AND #23 WERE REMOVED DUE TO INFECTION. THE PATIENT DID NOT BRUSH THE SURGICAL SITES DESPITE THE INSTRUCTIONS. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS.
Patient problems: Abscess; Unspecified Infection
MAUDE report 24802442 ↗InjuryApr 7, 2026Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.
Patient problems: Osteolysis
MAUDE report 24802352 ↗InjuryMar 24, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IMPLANT AT TOOTH SITE #33 WAS REMOVED DUE TO PERI-IMPLANTITIS AFTER 10 MONTHS OF PROSTHETIC TREATMENT.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 24680815 ↗InjuryFeb 23, 2026Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.
Patient problems: Inflammation; Osteolysis; Pain
MAUDE report 24421204 ↗InjuryJan 21, 2026Adverse Event Without Identified Device or Use Problem
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Pain
MAUDE report 24128326 ↗InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #11 AND #13 WERE REMOVED DUE TO INFECTION. THE PROCEDURE WAS NOT COMPLETED BY PLACING OTHER IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 24006541 ↗InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES # 11 AND # 13 WERE REMOVED DUE TO INFECTION. THE PROCEDURE WAS NOT COMPLETE WITH OTHER IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 24006124 ↗InjuryJan 6, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT COMPLAINED OF CONSTANT PAIN WITH THE IMPLANT AT TOOTH LOCATION #20. THE IMPLANT WAS REMOVED DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: PAIN.
Patient problems: Pain; Unspecified Infection
MAUDE report 23980186 ↗InjuryDec 10, 2025Loss of Osseointegration; Adverse Event Without Identified Device or Use Problem; Loss of Osseointegration; Adverse Event Without Identified Device or Use Problem
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Osteolysis; Sinus Perforation; Swelling/ Edema
MAUDE report 23766310 ↗InjuryNov 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANTS WERE REMOVED DUE TO PERI-IMPLANTITIS. THE PROCEDURE WAS NOT COMPLETED WITH OTHER IMPLANTS.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 23659837 ↗InjurySep 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITES #31 (FDI) AND #41 (FDI) LOST INTEGRATION AND WERE REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS AND EDEMA.
Patient problems: Osteolysis; Swelling/ Edema; Unspecified Infection
MAUDE report 23040278 ↗InjurySep 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION RECEIVED AT THE TIME OF THIS REPORT.
Patient problems: Inflammation; Pain; Swelling/ Edema
MAUDE report 23040063 ↗InjuryAug 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #23 WAS REMOVED DUE TO PERI-IMPLANTITIS. PATIENT REFERRED DISCOMFORT, PAIN, AND INFLAMMATION.
Patient problems: Discomfort; Osteolysis; Unspecified Infection
MAUDE report 22898824 ↗InjuryJul 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. TOOTH SITE #36. PATIENT REFERRED PAIN AND INFLAMMATION.
Patient problems: Inflammation; Osteolysis; Unspecified Infection
MAUDE report 22673905 ↗InjuryJun 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THERE WAS A SMALL BUMP/LESION PRESENT AROUND THE IMPLANT AT TOOTH SITE #12. THE CUSTOMER CONFIRMED PERIAPICAL BONE LOSS. THE IMPLANT WAS REMOVED.
Patient problems: Osteolysis
MAUDE report 22210361 ↗InjuryJun 13, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Discomfort; Inflammation; Pain
MAUDE report 22201102 ↗InjuryMay 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Erosion; Swelling/ Edema; Unspecified Infection
MAUDE report 22118279 ↗InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO BONE LOSS.
Patient problems: Osteolysis
MAUDE report 22066784 ↗InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #22 WAS REMOVED DUE TO PERI-IMPLANTITIS. ROUTINE IMPLANT PROTOCOL PERFORMED WITH PLACEMENT AT 35 NCM WITH COPIOUS IRRIGATION. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS, INFLAMMATION & SWELLING.
Patient problems: Erosion; Osteolysis; Unspecified Infection
MAUDE report 22063056 ↗InjuryMay 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #23 WAS REMOVED DUE TO PERI-IMPLANTITIS.
Patient problems: Osteolysis; Unspecified Infection
MAUDE report 22046823 ↗InjuryMay 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO BONE LOSS. SYMPTOMS AS A RESULT OF THE EVENT: INFLAMMATION. TOOTH LOCATION UNKNOWN.
Patient problems: Inflammation; Osteolysis
MAUDE report 22046353 ↗InjuryMay 15, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Inflammation; Pain
MAUDE report 22027828 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.