Materialise N V recalls

Materialise N V appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2023-08-09.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in ma…
  FDA Device · Class II · 2023-08-09 · Materialise N V
• MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit…
  FDA Device · Class II · 2023-07-26 · Materialise N V
• Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of gl…
  FDA Device · Class II · 2020-09-02 · Materialise N V
• TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013
  FDA Device · Class II · 2020-03-25 · Materialise N V
• TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001
  FDA Device · Class II · 2020-03-25 · Materialise N V
• Signature Patient-Specific Surgical Guides
  FDA Device · Class II · 2015-11-04 · Materialise N V
• Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides are intended to be used as part of the Signa…
  FDA Device · Class II · 2015-03-25 · Materialise N V