Materialise N.V.: Medical Device Recalls in 2023

According to to data from the FDA, there were 2 medical device recalls made by Materialise N.V. in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

• ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101
• MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01