A bone foundation guide system having a bone foundation guide with a foundation guide body forming an open surgical space connecting a top of the bone foundation guide body with a bottom of the bone foundation guide body, the bottom contoured to removably affix the bone foundation guide body to the bone of a dental implant surgical site, the body further contoured to guide the cutting of bone from a dental implant surgical site and supporting a dental implant surgical guide; the dental implant surgical guide contoured to removably mate to the bone foundation guide body; wherein a combination of the bone foundation guide and the dental implant surgical guide forms a double open-ended placement channel that passes through a plurality of guiding cylinders held in tandem alignment to aid in the placement of a dental implant that is anchored in a site remote from the mouth.

The present disclosure is directed to tools, systems and methods for recontouring/reshaping gum tissue by engaging a consumable tip on a powered tool to abrade/ablate excess or mal-contoured gum tissue to allow better visualization of the tooth/implant structure and reduce the periodontal pockets to provide improved access for cleaning by both the patient and clinician. In some embodiments, the powered tool may use vibrational movement, longitudinal reciprocating movement, rotational movement, reciprocating rotational movement, or a combination of any of the above movement schemes. In some embodiments, a consumable tip may be directed for cleaning tooth/implant surfaces and for recontouring/reshaping gum tissue. The powered tool itself may be constructed to allow the cooling water flow used for operation to be directed to the site where the procedure is carried out for irrigation or to be directed elsewhere at the user's selection to facilitate gum contouring procedures.

The subject matter of the instant invention relates to a dental implant surgical apparatus and system comprising a customized dental ridge augmentation matrix and one or, optionally, a plurality of dental implant surgical drill guides, and methods of use thereof.

A predetermined bone site in a patient selected for restoration is exposed, contacted with an aqueous, methylene blue containing phosphoric acid solution for a time period of at least 3 minutes but no more than about 15 minutes, and thereafter cleansed ultrasonically to remove any bacteria that may be present. Preferred phosphoric acid concentration in the aqueous solution is about 37 percent by weight.

A dental implant includes a body and a threaded surface. The body has an upper portion, a middle portion, and a lower portion. The upper portion of the body includes a generally cylindrical region. The lower portion of the body includes a generally inwardly tapered region. The middle portion of the body includes an outwardly extending bulge. A maximum outer diameter of the bulge is greater than (i) a maximum outer diameter of the upper portion and (ii) a maximum outer diameter of the lower portion. The threaded surface is on the body within at least the upper portion of the body, the bulge, and the lower portion of the body.

An intraosseous dental implant for the application of biologically active agents directly to the surrounding soft tissues and bone tissue, and their substitutes, is described. The implant enables the measurement of the newly formed or lost bone tissue volume immediately adjacent to the implant. Increasing the dynamics of osseointegration growth directly results in the possibility of reducing the duration of the entire treatment protocol. To increase dynamics of the osseointegration process, the type of material from which the implant is made, its design features, surface topography, as well as the formation of layered structures and coating applications, are described. The implant introduces growth factors and other biologically active factors that affect an increase in the dynamics of osseointegration strength. The entire implant or a porous section thereof can be produced by 3D printing through selective melting/sintering of biocompatible metallic, ceramic, or metallic-ceramic composite powders with laser or electron beams.

The invention relates to a bone implant (1) for correcting an incorrect position of a bone, the bone implant (1) having a first portion (2) for attachment to a first bone portion (3) and a second portion (4) for attachment to a second bone portion (5), the bone implant (1) being prepared so that, when fixed to the bone, it orients the first bone portion (3) and the second bone portion (5) with respect to one another and keeps said portions at a distance from one another, the bone implant (1) having such a geometry and being adapted so as to force a predetermined orientation of the second bone portion (5) relative to the first bone portion (3). The invention also relates to a method for producing such a bone implant (1).

Provided is a method of forming a customized alveolar bone tissue. The method includes obtaining first data having image information corresponding to an original alveolar bone of an alveolar bone defect, obtaining second data having image information on a defective portion of the alveolar bone defect, calculating third data having image information on a barrier membrane covering the alveolar bone defect by using the first data and the second data, and forming a barrier membrane artificial tissue corresponding to the barrier membrane by using the third data.

The invention relates to a method for the non-invasive fragmentation of residual biomaterial after bone augmentation, and to a device specifically adapted for said method.

Periodontal disorders such as disorders associated with a dental implant are treated. An average power for a laser is selected via a user interface on a tablet, along with a set of permissible laser parameters provided in response to the selected average power. A gingival trough or flap is created around the implant with the laser. Infected tissue is selectively ablated or denatured via photothermolysis, and a pocket is lased around the affected implant. Marginal tissues are compressed against the implant.