Eztetic™ CT3110Recalls & reported problems

Summary

The FDA's MAUDE database contains 64 adverse event reports that list this exact device (DI 00889024343870), received between Nov 20, 2019 and Sep 28, 2026 — classified as 62 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Component Missing” (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

Recent adverse event reports

The 25 most recent of 64 reports, in the reporter's own words as published by the FDA.

• InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that an implant was removed due to a peri-implantitis at tooth site 33.Pain was reported as a consequence.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 50914381 ↗
• InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that an implant was removed due to a bone loss. The patient noted a small bump on the gingiva near the implant placed in site #23. Radiographs revealed some bone loss. A flap was raised revealing #23 implant had significant buccal bone recession exposing several implant threads.Abscess, pain and inflammation were reported as a consequence.

  Patient problems: Abscess; Osteolysis; Pain

  MAUDE report 50798606 ↗
• InjuryJun 10, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE FIXTURE (IMPLANT) AT TOOTH SITE #7 WAS MOBILE AND WAS REMOVED DUE INFECTION AND BONE LOSS. THE SITE WAS CLEANED AND BONE GRAFTING AND COLLAGEN MEMBRANE WERE USED. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS.

  Patient problems: Abscess; Osteolysis; Unspecified Infection

  MAUDE report 25461692 ↗
• InjuryMay 26, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE (B)(6) WAS REMOVED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 25279192 ↗
• InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT AT TOOTH SITE 44 WAS REMOVED DUE TO INFECTION. PATIENT EXPERIENCED ABSCESS, PAIN AND PHLEGMON (INFLAMMATION).

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 24605621 ↗
• InjuryMar 12, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT AT TOOTH SITE 23 WAS REMOVED DUE TO INFECTION. PATIENT EXPERIENCED PAIN AND INFLAMMATION.

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 24578596 ↗
• InjuryFeb 20, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE #21 WAS REMOVED DUE TO INFECTION & BONE LOSS. PATIENT CAME IN WITH INFECTION AROUND IMPLANT. ORAL EVALUATION AND X-RAY FOR INFECTION. IMPLANT REMOVED & DEBRIDEMENT. PATIENT WILL RETURN FOR BONE GRAFT & 4 MONTHS LATER NEW IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 24405457 ↗
• InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AN IMPLANT AT TOOTH SITE # 11 WAS REMOVED DUE TO A PERI-IMPLANTITIS. ABSCESS WAS FOUND AROUND THE ZIMVIE ESTHETIC IMPLANT IN POSITION 11, WITH AN 8MM POCKET FOUND AROUND THE ENTIRE SURROUNDING OF THE IMPLANT. ABSCESS, PAIN AND INFLAMMATION WERE REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 23744775 ↗
• InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AN IMPLANT AT TOOTH SITE # 25 WAS REMOVED DUE TO A PERI-IMPLANTITIS. ABSCESS WAS REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 23744772 ↗
• InjuryOct 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 INFECTION. IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # XX LOST INTEGRATION DUE TO AN INFECTION AND WAS REMOVED. IMPLANT REMOVED TO RID THE INFECTION AND AVOID FURTHER BONE LOSS. WILL WAIT 4-6 MONTHS TO REPLACE IMPLANT DUE TO INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS, INFLAMMATION, PAIN & SWELLING.

  Patient problems: Inflammation; Pain; Unspecified Infection

  MAUDE report 23350937 ↗
• InjuryAug 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 SITE #27 WAS REMOVED DUE TO PERI-IMPLANTITIS. SYMPTOMS AS A RESULT OF THE EVENT: SWELLING AND BONE LOSS.

  Patient problems: Osteolysis; Swelling/ Edema; Unspecified Infection

  MAUDE report 22786896 ↗
• InjuryAug 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ERYTHEMA/EDEMA DISTAL TO #19 IMPLANT EXISTS. SITES HAVE HEALED BUT NOTED BONE LOSS #19D BASED ON NEW PA RADIOGRAPHY. RECOMMENDED IMPLANT REMOVAL AND REPLACEMENT. THE IMPLANT AT TOOTH SITE #19 WAS REMOVED DUE TO ALLERGIC REACTION AND BONE LOSS. SYMPTOMS AS A RESULT OF THE EVENT: EDEMA; INFLAMMATION; PAIN & SWELLING.

  Patient problems: Hypersensitivity/Allergic reaction; Osteolysis

  MAUDE report 22688303 ↗
• InjuryJul 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS IN THE VESTIBULAR REGION, IMPLANTS TRANSLUCENT THROUGH THE GINGIVA. TOOTH SITE (B)(6).

  Patient problems: Osteolysis

  MAUDE report 22680985 ↗
• InjuryJul 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT IMPLANT WAS REMOVED DUE TO BONE LOSS IN THE VESTIBULAR REGION, IMPLANTS TRANSLUCENT THROUGH THE GINGIVA. TOOTH SITE # 41.

  Patient problems: Osteolysis

  MAUDE report 22680971 ↗
• InjuryJul 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANTS AT TOOTH SITES #14 AND #15 WERE REMOVED DUE TO PERI-IMPLANTITIS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 22632260 ↗
• InjuryJun 30, 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 #4 WAS REMOVED DUE TO BONE LOSS.

  Patient problems: Osteolysis

  MAUDE report 22353048 ↗
• InjuryJun 25, 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; Osteolysis; Unspecified Infection

  MAUDE report 22327710 ↗
• InjuryApr 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #31 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS IN THE PER THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 21771702 ↗
• InjuryMar 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN AN UNKNOWN DENTAL POSITION FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT THE PROCEDURE WAS NOT CONCLUDED

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 21570957 ↗
• InjuryFeb 7, 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 LOCATION IS UNKNOWN.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 21332695 ↗
• InjuryNov 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT ATTENDED TO HAVE THE HEALING COLLAR. HE DIDN'T TAKE ANTIBIOTIC. GUM HEALED BUT NOT CLOSED. IMPLANT UR2 WAS ROTATING SO WAS REMOVED DUE TO INFECTION. INFLAMMATION WAS REPORTED AS A RESULT OF THE EVENT.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 20707536 ↗
• InjuryNov 18, 2024Adverse 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 INFECTION. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS AND PAIN.

  Patient problems: Erosion; Pain; Unspecified Infection

  MAUDE report 20706251 ↗
• InjuryOct 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED AT UNCOVERING, INFECTION PRESENT. PER INDICATED: SURGICAL/MEDICAL INTERVENTION REQUIRED FOR PERMANENT DAMAGE: NO. ADDITIONAL APPOINTMENT REQUIRED: NO. SYMPTOMS AS A RESULT OF THE EVENT: NONE REPORTED. WAS THE PROCEDURE COMPLETED USING ANOTHER IMPLANT OR ANOTHER DEVICE: NO.

  Patient problems: Unspecified Infection

  MAUDE report 20543257 ↗
• InjuryJul 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DENTIST DETECTED CIRCUMFERENTIAL BONE LOSS AROUND TOOTH SITE #12, MORE PRONOUNCED IN THE VESTIBULAR AREA. IMPLANT WAS REMOVED. ADDITIONAL APPOINTMENT REQUIRED: WAITING FOR HEALING TO TRY ANOTHER IMPLANT.

  Patient problems: Osteolysis

  MAUDE report 19772823 ↗
• InjuryJun 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT AT TOOTH SITE # 24 WAS REMOVED DUE TO INFECTION. PATIENT HAD INFECTION AND DRAINAGE. SYMPTOMS AS A RESULT OF THE EVENT: ABSCESS.

  Patient problems: Unspecified Infection

  MAUDE report 19520121 ↗