Lateral Mandibular Angle™ Size: 4/10, LeftRecalls & reported problems
Implantech Associates, Inc. · Mandibular Implant · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M724TMA0410L1), received between Jun 16, 2022 and Jun 16, 2022 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Bacterial Infection1
- Failure of Implant1
- Fluid Discharge1
- Hemorrhage/Blood Loss/Bleeding1
- Physical Asymmetry1
- Swelling/ Edema1
- Wound Dehiscence1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 16, 2022Adverse Event Without Identified Device or Use Problem
THE PATIENT/COMPLAINANT REPORTED RECEIVING SEVERAL FACIAL IMPLANTS, THEN SUBSEQUENTLY EXPERIENCED THE STITCHES AT SITE OF LEFT SIDE MANDIBULAR IMPLANT OPENING WITH AN OUTFLOW OF FULID AND BLOOD (APPROXIMATELY 5 DAYS POST-OP). SEVEN (7) DAYS POST-OP, THE DOCTOR SEWED UP THE INCISION SITE. FOUR (4) WEEKS POST-OP, THE STITCHES HAD REOPENED, AND WERE AGAIN SEWED UP UNDER LOCAL ANESTHESIA. FIVE (5) WEEKS POST-OP, THE DOCTOR SEWED UP THE INCISION FOR THE THIRD TIME BECAUSE THEY HAD AGAIN REOPENED. ALMOST 7 WEEKS POSTOP, PATIENT REPORTED TO PHYSICIAN THAT THE STITCHES HAD OPENED MORE THAN EVER AND THE IMPLANT WAS VISIBLE. APPROXIMATELY EIGHT (8) WEEKS POST-OP, PATIENT HAD A SECOND OPERATION UNDER TOTAL ANESTHESIA, WHERE THE DOCTOR "REMOVED THE IMPLANT, RECONSTRUCTED THE AREA, STERILIZED THE IMPLANT CLINICALLY HIMSELF AND PLACED IT AGAIN, PLACING 1 SCREW INTRAORALLY". THREE (3) MONTHS AFTER THE SECOND SURGERY, THE POST-OPERATIVE SWWELLING HAD NOT SUBSIDED. THE PATIENT HAD LOST FAITH IN THE ORIGINAL DOCTOR, AND SAW ANOTHER PHYSICIAN WHO SUGGESTED A POSSIBLE INFECTION. PATIENT SAW ANOTHER DOCTOR WHO DIAGNOSED ASYMMETRY IN THE FACE WITH SEVERE SWELLING ON THE LEFT SIDE. THE DOCTOR PR
Patient problems: Bacterial Infection; Failure of Implant; Fluid Discharge; Hemorrhage/Blood Loss/Bleeding; Physical Asymmetry; Swelling/ Edema; Wound Dehiscence
MAUDE report 14714156 ↗
Other Prosthesis, Chin, Internal devices
- MEDPOR 5444-0-310Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL6 reports
- MEDPOR 5444-0-510Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 5444-0-410Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 82007Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 5444-0-110Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL3 reports
- MEDPOR 5444-4-310Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL3 reports
- Conform™ Extended Anatomical Chin Size: MediumImplantech Associates, Inc. · Prosthesis, Chin, Internal3 reports
- MEDPOR 80010Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL3 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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