The present disclosure provides a dental implant configured to be inserted in a hole in jaw bone and to be at least partially situated in the bone tissue when implanted and includes: a coronal region, an apical region, a longitudinal axis extending from the coronal region of the dental implant to the apical region of the dental implant; an implant surface configured to form an interface between an implant material and the oral environment/surrounding tissue and a surface layer formed on at least part of the implant surface, the surface layer including crystalline titanium oxide in the anatase phase and wherein the surface area roughness Sa and the pore size of the implant surface on which said surface layer is formed increase from the coronal region toward the apical region of the dental implant along the longitudinal axis.

The present disclosure relates to a medical cement composition containing calcium silicate in an amount of less than 20 wt % of a total weight of the composition, with a lithium salt being added thereto. The medical cement composition of the present disclosure has a low compressive strength of 12 MPa or less, after being hardened, for easy removal, excellent stability in storage, and high bioactivity.

The present disclosure relates to a medical cement composition containing calcium silicate in an amount of less than 20 wt % of a total weight of the composition, with a lithium salt being added thereto. The medical cement composition of the present disclosure has a low compressive strength of 12 MPa or less, after being hardened, for easy removal, excellent stability in storage, and high bioactivity.

A biocompatible composite material for controlled release is disclosed, comprising a biocompatible metal oxide structure with a loaded network of pores. The pore network of the biocompatible composite material is filled with a uniformly distributed biologically active micellizing amphiphilic molecule, the size of these pores ranging from about 0.5 to about 100 nanometers. The material is characterized in that when exposed to phosphate-buffered saline (PBS), the controlled release of the active amphiphilic molecule is predominantly diffusion-driven over time.

A biocompatible composite material for controlled release is disclosed, comprising a biocompatible metal oxide structure with a loaded network of pores. The pore network of the biocompatible composite material is filled with a uniformly distributed biologically active micellizing amphiphilic molecule, the size of these pores ranging from about 0.5 to about 100 nanometers. The material is characterized in that when exposed to phosphate-buffered saline (PBS), the controlled release of the active amphiphilic molecule is predominantly diffusion-driven over time.

The invention relates to a scan abutment (2) for determination of the position of the plane of the front face (1.1) of a dental endosseous implant (1), wherein the abutment (2) has a longish, hollow shaft (4) and a base (3) at the bottom side (4.2) of the shaft (4), and the base (3) with at least a part of its bottom side (8.2) is attachable onto the front face (1.1) of the implant (1), wherein the base (3) has a recess (9) extending from the upper side (8.1) to the lower side (8.2) of the base (3), wherein the longish, hollow shaft (4) has from a side wall (10) having at least one through hole (5a) at its outer periphery, wherein the through hole of the side wall (10) extends from the bottom side (4.2) of the shaft (4) to the upper side (4.1) of the shaft, thereby forming a planar surface (6) in the plane (12) between shaft (4) and base (3).

The invention relates to a scan abutment (2) for determination of the position of the plane of the front face (1.1) of a dental endosseous implant (1), wherein the abutment (2) has a longish, hollow shaft (4) and a base (3) at the bottom side (4.2) of the shaft (4), and the base (3) with at least a part of its bottom side (8.2) is attachable onto the front face (1.1) of the implant (1), wherein the base (3) has a recess (9) extending from the upper side (8.1) to the lower side (8.2) of the base (3), wherein the longish, hollow shaft (4) has from a side wall (10) having at least one through hole (5a) at its outer periphery, wherein the through hole of the side wall (10) extends from the bottom side (4.2) of the shaft (4) to the upper side (4.1) of the shaft, thereby forming a planar surface (6) in the plane (12) between shaft (4) and base (3).

The present invention relates to a dental composition and a dental kit comprising a polymerisable adhesive free of a photoinitiator, and a self-cure composite restorative including a redox initiator system. The dental composition cures upon contact between the self-cure composite restorative and the adhesive, to thereby form a dental restoration. The present invention also relates to a method of applying the dental composition, and methods of replacing a dental amalgam with the dental composition, or dental kit, of the present invention.

The present invention relates to a dental composition and a dental kit comprising a polymerisable adhesive free of a photoinitiator, and a self-cure composite restorative including a redox initiator system. The dental composition cures upon contact between the self-cure composite restorative and the adhesive, to thereby form a dental restoration. The present invention also relates to a method of applying the dental composition, and methods of replacing a dental amalgam with the dental composition, or dental kit, of the present invention.

Provided is a curable composition that has a sufficient pot life and does not cause a significant delay in curing time even after long-term storage at room temperature or higher. A separately packed curable composition includes: (A) a first pack containing: (a1) a polymerizable monomer having no acidic group, (b) a polymerizable monomer having an acidic group, and (c) a transition metal compound; and (B) a second pack containing: (a2) a polymerizable monomer having no acidic group, (d) an aromatic amine compound, and (e) at least one compound selected from sulfinic acid and a salt thereof.