4 results · 54ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

32MM MOD HEAD COCR -6MM NECK

FDA Adverse Event
Injury ·BIOMET FRANCE SARL·Product code JDI·October 23, 2014

OPTIPAC 40 REFOBACIN BN CMT R

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LOD·October 27, 2020

Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge augmentation/reconstruction, " Sinus elevation, " Filling of resection defects in benign bone tumor, bone cysts, or other defects in the alveolar ridge or wall, " Filling of bone defects after apicectomy, " Filling alveoli after tooth extraction. This product should not be used in non-peridontal mandibular applications.

FDA Enforcement
Class II ·Terminated·Biomet France SARL·February 17, 2016

Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge augmentation/reconstruction, " Sinus elevation, " Filling of resection defects in benign bone tumor, bone cysts, or other defects in the alveolar ridge or wall, " Filling of bone defects after apicectomy, " Filling alveoli after tooth extraction. This product should not be used in non-peridontal mandibular applications.

FDA Recall
Terminated ·Biomet France SARL Plateau de Lautagne Valence Cedex·Product code LYC·January 21, 2016