Extended Anatomical Chin Size: SmallRecalls & 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 M724EACS1), received between Nov 21, 2024 and Nov 21, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Bacterial Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
COMPLAINANT REPORTED THAT PATIENT HAD CHIN IMPLANT EXPLANTED AFTER SLIGHTLY MORE THAN 4 MONTHS DUE TO INFECTION. ABOUT 14 WEEKS POST-OP, THE PATIENT REPORTED SWELLING. A CYST AT THE SITE WAS DRAINED AND CULTURED, AND STAPH AUREUS WAS IDENTIFIED. PATIENT WAS TREATED WITH ORAL BACTRIM WHICH BRIEFLY RESOLVED SYMPTOMS, HOWEVER THE CYST CAME BACK (REDNESS AND SWELLING). IT WAS CULTURED AGAIN AND STAPH AUREUS WAS IDENTIFIED. SHORTLY AFTER, DEVICE WAS EXPLANTED. REPORTING PHYSICIAN'S OFFICE NOW INDICATES SYMPTOMS APPEAR TO BE RESOLVED.
Patient problems: Bacterial Infection
MAUDE report 20746993 ↗
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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