|BioPlant, a dental bone grafting material. BioPlant
has been assigned the product code LYC (Bone Grafting Material, Synthetic) by the
FDA and is classified as a Class II Medical Device.
BioPlant is a Class II Medical Device. The Device Listing Number is 0007254.
BioPlant is a synthetic, multipurpose bone-grafting material intended to be used in dental applications to maintain and restore the bony alveolar ridge in post-extraction tooth-root sockets or after oral surgery, ridge preservation, ridge augmentation, augmentations in the maxillary sinus, repair of periodontal defects and bone voids associated with dental implant placement.
||The BioPlant part numbers and lot numbers affected by this recall are as follows:
ÿProduct Description Part Numbers Lot Numbers
SioPlant Curved Syringe, 0.125g 216110 All Production
SioPlant Curved Syringe, 0.25g 216112
SioPlan! Curved Svrinoe, 0.50<1 216114 Lots Within Shelf-Life
BioPlant Curved Svrinoe, 0.250 216132 20k
BioPlant Intro Pack 216112S
||The firm initiated the recall becaue disturbing the BioPlant product soon after it is placed may halt or delay the ossification process.