A dental restoration method comprising a step of determining a positioning of a dental implant (60), integrated into a bone structure (62) of an individual, from the identification and positioning of a one-piece healing member (10), attached at one of the ends of same in the implant (60), the healing element (10) comprising a side surface (13) intended to be integrated into a gum in order to shape the gum during the healing of same, and an end surface (14), a part of the side surface (13) and of the end surface (14) forming an emergent surface, intended to remain outside the gum, that is asymmetrical relative to at least a perpendicular median plane.

An abutment system is for attachment to a dental implant having a threaded bore and for engaging the surrounding gingival tissue. The abutment system includes a base and a polymeric abutment cap. The base includes a lower region and an upper region. The lower region includes an anti-rotational feature for non-rotationally mating with one of the dental implants. The upper region includes a first anti-rotational structure and a first axial retention structure. The polymeric abutment cap has a second anti-rotational structure for mating with the first anti-rotational structure and a second axial retention structure for mating with the first axial retention structure. The abutment cap has an upper surface that includes information markers. The information markers define a unique code that provides information concerning the abutment cap and the underlying dental implant.

An embodiment of the present invention provides a dental implant packaging container comprising: an implant fixing unit to which an implant can be detachably coupled; a sealing cap including the implant fixing unit; and a casing, wherein: the sealing cap and the casing form an inner space together; the casing has a hollow cylindrical shape and is partially opened; the inner space is formed by coupling the sealing cap to the opened portion of the casing; and the implant is breakably coupled to the implant fixing unit.

A method for securing a dental implant within a dental bone cavity is disclosed. The method may include inserting a dental wedge into the dental bone cavity and allowing bone tissues to grow toward and at least partially surround the dental wedge. Dental implantation systems for implementing the method are also disclosed. The system can include a dental wedge adapted to be inserted into a dental bone cavity.

A computer based method is used to design a healing cap of an implant. The method is based on a 3D computer plan of the implant that includes digital representations of positions of implants in the mouth of the patient. The method comprises loading 3D implant plan into a computer and combining the 3D implant plan with information about a prosthetic setup. The method determines a marginal edge of a healing cap of an implant based on a 3D representation of the existing patient anatomy, the 3D implant plan and the prosthetic set-up. The healing cap is then manufactured to the custom design.

An alveolar membrane includes: a connecting portion being provided thereon with a through hole for an artificial toothroot to pass therethrough; a capping portion having its one end connected to the connecting portion and including a plurality of openings; and a fixing portion being located at an opposite end of the capping portion and having at least one digit that has a tip to be fixed in osseous tissue or between osseous tissue and soft tissue. With the connecting portion and the fixing portion at its two ends both fixed, the alveolar membrane firmly holds the osseous graft in position.

Provided is a method of controlling local release of target compounds by patterning a hydrogel carrying a bone morphogenetic protein as the target compounds on a nanoporous membrane. The nanoporous membrane is capable of controlling local release of the bone morphogenetic protein as a carrier of the bone morphogenetic protein while performing a basic function of the membrane of preventing infiltration of connective tissue, and thus, there is an advantage in that the nanoporous membrane can facilitate generation of controlled bone in a local region.

Methods of taking an impression or scan of a patient's oral cavity without requiring removal of a healing cap coupled within the implant in the subgingival void. The method may include providing an anatomical healing cap received within the subgingival void of a given tooth position, where the anatomical healing cap is coupled into an implant in the void. A scanning body or an impression post is inserted into an open end (e.g., the hollow core) of the anatomical healing cap, in-situ, with the anatomical healing cap positioned in the subgingival void, and the implant thereunder (or thereover for a maxillary tooth position). The scanning body or impression post is used as a reference in making the impression or scan. Because this is done without requiring removal of the healing cap, further collapse of the gingival tissue surrounding the void is prevented.

A dental implant assembly may be provided with a spacer removably attachable to a dental implant, a cap removably attachable to the spacer, and a surgical barrier that may be at least partially disposed between the cap and the spacer. The spacer may include a first end configured to engage with the dental implant and a second end configured to engage with the cap. The second end may further include a tool connection region. The surgical barrier may include an outer membrane and an inner mesh enclosed within the outer membrane. A cap head may be provided with a lower surface configured to engage with the surgical barrier. A cap body may be provided with a threaded profile engageable with a threaded connection of the second end of the spacer. At least part of the surgical barrier may be sandwiched between the spacer and the lower surface of the cap.

An anatomical healing abutment is configured to connect to a dental implant. The healing abutment has a body portion which includes at least three reference marks that provide data to orient the connection axis of the abutment with the that of the dental implant so that certain conventional steps, including healing abutment manipulation, multiple scans, and the taking of impressions, can be eliminated, thereby saving time and effort on the part of the practitioner.