| Nom | Classification | Fabricant | Classe de risque | Pays | Source |
|---|---|---|---|---|---|
| Device Recall Tumark Q | General and Plastic Surgery Devices | Somatex Medical Technologies GmbH | 2 | United States | USFDA |
| Sinus-SuperFlex-635 | optimed Medizinische Instrumente GmbH | Germany | BAM | ||
| the OptiSplint Endoprosthesis | optimed Medizinische Instrumente GmbH | Germany | BAM | ||
| 200 mm sinus-SuperFlex-635 self-expanding nitinol stent system | optimed Medizinische Instrumente GmbH | Germany | BAM | ||
| Stent system sinus-Carotid-RX and sinus-Carotid-Conical-RX | optimed GmbH | Germany | BAM |