An endosseous dental implant assembly includes a dental implant including an abutment portion for connecting to a tooth crown and a hollow base portion defining a cavity therein, and a bio-supportive or biodegradable scaffold carried by the hollow base portion of the dental implant in the biomimetic approach. The abutment portion is formed integrally with the hollow base portion. The scaffold is impregnated with regenerative stem cells, growth factors, biomorphic proteins, or autogenous cells. In the osseointegrated approach, bone graft material can be carried to the extraction socket without a scaffold.

The porous three-dimensional structure of the implant is made as a three-dimensional body with open through pores and one-side open pores distributed evenly on the internal surface of open pores and connected to the internal surface. Sizes of pores are randomly distributed in the range of 150-300 μm. A reinforcing element is made from titanium or titanium alloy as a mesh with the protrusions evenly distributed on the outer surface of the mesh, and is located on the surface of the three-dimensional body. The method of manufacture and method of installation of one of the variants of the dental implant with the possibility of press fit in the jaw bone immediately after extraction of the tooth without arrest of bleeding are based on the porous three-dimensional structure claimed as well.

A dental implant supported on the cortical bone is implanted in the socket from which the tooth was extracted, if this hole still exists, or in the remaining socket when the tooth was extracted some time before, or alternatively in a hole made for placement of the implant, at cortical bone level, and externally, between the cortical bone and the gingiva, slightly embracing the mandible and the maxilla.

In one embodiment, in order to enhance the fixation and implant lifetime vascularization, the implant of the present disclosure for fitting in an intraosseous zone of a dental socket includes a plurality of raised platforms with a flat top such that said tops form an external surface of the implant for contacting with the intraosseous zone and the spaces between said platforms form a network of channels for revascularisation fluid flow with capillarity properties.

The present invention relates to a customized or standardized bionic implant and its manufacturing, especially for dental applications. According to the first variant of the invention, the implant is characterized in that its single-component anchor possesses at least two bionic arms (2) tapering circumferentially, thereby creating at least one pointed (5) and/or linear (6) blade on each arm (2). According to the second variant of the implant, the single-component anchor possesses at least two bulging arms (2) forming at least one protrusion (4) on each of them. The manufacturing method depends on whether the implant is standardized, new and customized or is a modification of an implant selected from a digital library of standardized implants. Physical form of embodiments of the anchor may be printed in a 3D printer. In the case of customized implants, the process commonly comprise obtaining tomographic images of the biological target. In the case of designing a new implant, a panoramic curve/curves and panoramic surface are set and become the basis for the arms (2) of the implant's virtual anchor.

An anatomical dental implant arranged to be implanted in a naturally occurring cavity of the jawbone, the implant comprising at its apical side a root part arranged to anchor the implant in the cavity and at its occlusal side an abutment part arranged for supporting a dental prosthetic element, wherein the root part comprises an outer surface arranged to come into contact with the cavity walls, and wherein the root part comprises an outer section adjacent to the outer surface of the root part, wherein the outer section of the root part is arranged to deform plastically upon insertion of the root part into the cavity such that the root part substantially conforms to the shape and size of the cavity.

A dental implant for supporting periodontal tissue and the supporting bone is provided. The dental implant includes an implant member with inner canal for insertion into a periodontal bone socket, and an anchoring assembly. The anchoring assembly includes a first fastening element and radially equidistant cylindrical members. The first fastening element engages the implant member within the hollow axial cavity. The root section includes through-holes for radially and forcibly sliding the cylindrical members through them. When the first fastening element apically advances within the hollow axial cavity, the cylindrical members generate an anchoring force to anchor the dental implant.

Embodiments of the disclosure relate to implantable objects and guiding devices, as well as recipient site preparation instruments, bone-implantable materials, and methods of fabrication and use thereof.

A human implant includes at least one osteoconductive scaffold and at least one main carrier. The at least one osteoconductive scaffold is made of a metal material, is manufactured by 3D printing, and has at least one connecting portion, at least one separation element, and a proliferation portion. The at least one connecting portion is porous. The at least one separation element is disposed on one of two sides of the at least one connecting portion. The proliferation portion is disposed on one of two sides of the at least one separation element away from the at least one connecting portion, wherein osteoblasts proliferate in the proliferation portion. The at least one main carrier is made of a medical macromolecular material and is mounted to the at least one connecting portion being porous, such that the at least one main carrier is mounted to the at least one osteoconductive scaffold.

Dental implants may be designed using a three-dimensional scan of an extracted tooth root and/or a corresponding socket site. The dental implant may include a root portion designed to sit below the patient's gum line, a connector portion positioned above the root portion and designed to sit above a rim of a socket site and/or gum line, and an abutment portion positioned above the connector portion upon which a crown may be placed. The root portion may include three sections that correspond to three areas of a three-dimensional scan of an extracted tooth root. The first and third sections of the implant may have a size and shape that corresponds to a first and third portions of the three-dimensional scan, respectively. A circumference of the second section of the implant may be smaller than a corresponding circumference of the second section of the three-dimensional scan of the tooth root.

Embodiments of the disclosure relate to implantable objects and guiding devices, as well as recipient site preparation instruments, bone-implantable materials, and methods of fabrication and use thereof.