MAUDE Adverse Event Report: IMPLANTECH ASSOCIATES, INC. CONFORM MANDIBULAR ANGLE (TM); MANDIBULAR IMPLANT

Model Number	N/A
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	09/20/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Method: actual device was not returned, so implantech reviewed production records, as well as performing trend analysis.(there have been no other reports associated with this lot , or on the cma-14l catalog number.Review found event(s) are not occurring more frequently or severely than anticipated.) results: no device problem was found.Conclusion: both displacement and poor wound healing are know, inherent risks with facial implant surgery, and are addressed in the labeling for the product.
Event or Problem Description
Complainant reported that patient who had mandibular angle implants placed, subsequently had implants explanted bilaterally approximately 10 weeks post-operatively.This report is regarding the left side implant.(see mdr # 2028924-2021-00007 for report on the rights side implant.).

• Brand Name: CONFORM MANDIBULAR ANGLE (TM)
• Common Device Name: MANDIBULAR IMPLANT
• Manufacturer (Section D): IMPLANTECH ASSOCIATES, INC.; 6025 nicolle street, suite b; ventura CA 93003
• MDR Report Key: 12661069
• Report Number: 2028924-2021-00006
• Device Sequence Number: 11815071
• Product Code: FWP
• UDI-Device Identifier: M724CMA14L1
• UDI-Public: M724CMA14L1
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K905268
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2021
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/19/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 06/26/2025
• Device Model Number: N/A
• Device Catalogue Number: CMA-14L
• Device Lot Number: 888511
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/06/2021
• Initial Report FDA Received Date: 10/19/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 35 YR