A dental implant including a first, apical portion for inserting into bone, and a second, top-side portion, starting at a level of bone surface and higher, including a stricture of the dental implant diameter, relative to a diameter of the top-side portion, for at least part of the top-side portion. Related apparatus and methods are also described.

An implant device has an exterior portion forming an exterior surface of the implant. The exterior portion is made of a porous material defining passages through the exterior portion. An inner portion has an outer surface with a treated area that is accessible from the exterior surface through the passages. The treated area has a treatment for direct attachment to bone or soft tissue.

The invention relates to a bioinert body having a base body, which grows to a multiple of its volume when hydrated. The base body substantially consists of dried laminaria parts, which also develop a local antibacterial effect due to the iodine content. The bioinert body is suitable for application in a method of tissue augmentation.

A dental implant includes a crown socket for supporting a prosthetic tooth, the crown socket comprising a first longitudinal axis for supporting the prosthetic tooth in an anatomically correct shape; an abutment; and an implant post having a second longitudinal axis coinciding with a third longitudinal axis of an osteotomy; the first longitudinal axis and the second longitudinal axis are not coincident.

A custom dental implant and a method and system for making the custom dental implant having one or more energy storing devices that deflect during installation and expand to provide stability after insertion in a natural dental socket of a patient.

An implant fixture is disclosed. The implant fixture contains an elongated shaft section, and a head section comprising a concavity along the head section's perimeter, wherein the concavity provides an area for bone growth therein to compensate for jawbone deterioration adjacent to the implant fixture due to craniofacial growth.

A dental prosthesis attachment system is for an endosseous dental implant. The dental prosthesis attachment system includes: a removable dental prosthesis; a dental prosthesis portion secured to the removable dental prosthesis; and a dental implant portion securable to the dental implant and removably engageable with the dental prosthesis portion. The dental prosthesis portion includes an open-ended dental prosthesis sleeve having an outer surface and an inner cavity. The outer surface is secured to the dental prosthesis and the inner cavity is lined with a retention material defining an inner peripheral wall having at least one of a protrusion and a recess. The dental implant portion includes an attachment pillar removably insertable within the inner cavity of the dental prosthesis portion. The attachment pillar has a peripheral wall provided with at least one of a protrusion and a recess removably interlocked with the at least one of the recess and the protrusion on the inner peripheral wall of the inner cavity.

A fixture (10) to be embedded in a bone (H), comprising: a fixture body (11) through which a central hole (13) penetrates over the entire length thereof; and a cap body (21) which closes an opening on a root end side of the central hole (13). The cap body (21) has a first shaft section (24) to be fitted into the central hole (13). The central hole (13) has a first tapered hole section (14) which decreases in diameter from the root end side toward a top end side, and the cap body (21) has a first tapered shaft section (25) to be fitted into the first tapered hole section (14).

A dental implant including an implant body having a top surface, and at least one non-annular cutaway portion longitudinally extending downwardly from the top surface along one side of the body and outwardly to the periphery, and a method for making the implant. The implant body preferably includes a body portion and a head portion integrally formed with the body portion, the body portion has a periphery and the head portion has a non-circular periphery, and the periphery of the head portion is smaller than the periphery of the body portion.

An implant or endoprosthesis suitable to be implanted in human or animal tissue includes two (or more than two) parts to be joined in situ. Each one of the parts includes a joining location, the two joining locations facing each other when the device parts are positioned for being joined together, wherein one of the joining locations includes a material which is liquefiable by mechanical vibration and the other one of the joining locations includes a material which is not liquefiable by mechanical vibration and a structure (e.g. undercut cavities or protrusions) suitable for forming a positive fit connection with the liquefiable material. The joining process is effected by pressing the two device parts against each other and by applying ultrasonic vibration to one of the device parts when the two parts are positioned relative to each other such that the two joining locations are in contact with each other.