International safety notice

Exoplan. Cuando se utiliza para la planificación de casos totalmente guiados utilizando las bibliotecas de implantes Bicon, sleeve Bicon y kits Bicon.

Spain / AEMPS · ESP · May 25, 2023

Key facts

Title Exoplan. Cuando se utiliza para la planificación de casos totalmente guiados utilizando las bibliotecas de implantes Bicon, sleeve Bicon y kits Bicon.
Regulator Spain / AEMPS
Country ESP
Brand Exoplan. Cuando se utiliza para la planificación de casos totalmente guiados utilizando las bibliotecas de implantes Bicon, sleeve Bicon y kits Bicon.
Manufacturer Exocad GmbH, Alemania.
Models 17600, 51-53, 2023-04, 91.822.52.89, SOFTWARE2.3, PMC8762866, DE-MF-000007341, 260-940-380, 2.POSIBLE, 4260521365019, 4.0BICON®, 2023-251 and 24 more
Event type Safety Notice
Date May 25, 2023

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices