Conform™ Extended Anatomical Chin Size: LargeRecalls & reported problems
Implantech Associates, Inc. · Chin 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 M724CEACL1), received between Sep 16, 2020 and Sep 16, 2020 — 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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Inflammation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 16, 2020Appropriate Device Problem Term/Code Not Available
COMPLAINANT REPORTED THAT PATIENT RETURNED TO OFFICE 1 YEAR POST-OP WITH AN INDENTATION IN THE MIDDLE OF THE CHIN DIRECTLY UNDER THE INCISION LINE. APPROXIMATELY 14 MONTHS POST-OP, COMPLAINANT PERFORMED REVISION PROCEDURE ON THE PATIENT IN WHICH THE SKIN AND GRANULATION TISSUE OVERERLYING THE IMPLANT WERE EXCISED. PATHOLOGY CAME BACK AS ACUTE AND CHRONIC INFLAMMATION. THE IMPLANT WAS NOT REMOVED, AND PROCEDURE WENT WELL. (NOTE: AS PHYSICIAN HAS NOT OFFERED AN OPINION ON WHETHER THIS PROCEDURE CONSTITUTED SURGICAL INTERVENTION NEEDED TO PRECLUDE PERMANENT IMPAIRMENT OF A BODY FUNCTION OR PERMANENT DAMAGE TO A BODY STRUCTURE, OR WHETHER THE DEVICE CAUSED OR CONTRIBUTED TO THE EVENT, IMPLANTECH HAS ELECTED TO REPORT THIS EVENT.)
Patient problems: Inflammation
MAUDE report 10541035 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page