Conform Mandibular Angle™ Size: 8, LeftRecalls & reported problems
Implantech Associates, Inc. · Mandibular Implant · Class 2 · Implant
Data updated Oct 16, 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 M724CMA8L1), received between Feb 25, 2020 and Feb 25, 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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 25, 2020Adverse Event Without Identified Device or Use Problem
COMPLAINANT REPORTED THAT PATIENT COMPLAINED OF SWELLING & A BAD TASTE IN HIS MOUTH 3 WEEKS AFTER BEING IMPLANTED BILATERALLY. SUBSEQUENTLY, THE PATIENT HAD THE LEFT SIDE DEVICE EXPLANTED DUE TO A DIAGNOSIS OF INFECTION. NO CULTURE WAS TAKEN, HOWEVER PUS WAS FOUND DURING EXPLANT SURGERY. COMPLAINANT REPORTS PATIENT WAS SEEN 16 DAYS AFTER EXPLANT, AND SYMPTOMS HAD RESOLVED. (NOTE: IN (B)(6) 2019, PATIENT DID RECEIVE INJECTIONS OF "BELLAFILL" IN THE SAME REGIONS WHERE MANDIBULAR IMPLANTS WERE SUBSEQUENTLY PLACED.)
Patient problems: Unspecified Infection
MAUDE report 9752917 ↗
Other Prosthesis, Chin, Internal devices
- MEDPOR 5444-0-310Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL6 reports
- MEDPOR 5444-0-410Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 82007Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 5444-0-510Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL4 reports
- MEDPOR 80010Stryker Leibinger GmbH & Co. KG · PROSTHESIS, CHIN, INTERNAL3 reports
- MEDPOR 5444-4-410Stryker 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
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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