170 results about "Alveolar ridge" patented technology

The invention relates to a custom-fit implantable surgical guide (1) and an associated milling tool (4), which is positioned in straddling on the alveolar ridge (7) of a maxillary or mandible arch (2) and comprises at least one drilling barrel (11) for axially guiding said milling tool (4), wherein said barrel (11) is laterally open and at least one part of the internal surface thereof (17) and at least one part of the external surface of the milling tool (4) interact and axially maintain the entire milling tool (4) with respect to the barrel (11). Said invention makes it possible to carry out high precision osteotomies for lateral insertion dental implants.

A multi-function brush for an overdenture includes a brush handle having a head end and a tail end. The head end has a first surface and a second surface opposite to the first surface. The first group of brushes is provided on the first surface of the head end. The second group of brushes is provided on the second surface of the head end. The third group of brushes is provided on the tail end. With these three groups of brushes having different locations, specifications and indications, an overdenture user can clean the tissue surface and the denture surface of the overdenture, the male part of the dental attachments provided on the tissue surface, and the female part of the dental attachments provided on alveolar ridge or roots by this single brush. Thus, the present invention really has convenience and practicability, and the money for buying different toothbrush and denture brush is saved.

A method and apparatus is disclosed for providing implants in the upper jaws of a person. A sleeve is inserted through the alveolar ridge to the maxillary sinus. The sleeve is used to raise the subantral membrane and form a cavity. A filler, such as a bone growth stimulant is injected through the sleeve into the cavity. In the process, the sleeve also can cut and / or condense the bone around itself so that the bone can hold an implant. Optionally, the bone growth stimulant is also introduced into the bone surrounding the sleeve. During the injection, the pressure within the sleeve or the cavity is monitored to detect and prevent the rupture of the subantral membrane.

A removable denture system comprising a support beam fixedly attached to the individual's alveolar ridge above the mucous membrane by a plurality of dental implants, and a denture generally conforming with the dental parameters of the individual and integrated with a super-structure. The super-structure comprises at least a portion shaped in confirmation with the support beam, and a denture locking arrangement for removably though fixedly articulating the denture to the support beam preventing unintentional disengagement of the denture.

A method for inserting a flowable material adjacent the alveolar ridge bone through an elongated tube having an a side perforation. The elongated tube can be a dental implant.

An orthodontic distalizing apparatus comprises at least one force generating element positioned intermediate a force dissipating element secured to the hard palate and / or alveolar ridge and a first tooth (e.g., a molar) that is being distalized. The at least one force generating element is positioned to apply a distalizing force on the molar in a direction substantially along a longitudinal axis of the dental arch and at a low level of the basal gingiva. The at least one force generating element may be configured to prevent inadvertent disassembly thereof during installation, adjustment and / or conversion of the apparatus between an active and a passive state. In addition, the at least one force generating element may be configured to be reversibly convertible between an active state and a passive state without requiring removal of the device from the patient's mouth. Moreover, the at least one force generating element may be configured to provide a continuous activation force of substantially constant magnitude during distalization of the molar. The apparatus may also be constructed so that the force dissipating element is connected to at least one anchoring tooth by a slidable coupling that absorbs all reaction forces transmitted substantially along a direction of the longitudinal arch. A second force dissipating element may be positioned intermediate the force dissipating element and a second tooth (e.g., a bicuspid) to facilitate the closing of any gaps that are created following distalization of the molar. A method of converting an orthodontic distalizing apparatus between an active and a passive state is also provided.

A biocompatible, self-supporting, curved, collagen membrane adapted to be secured by bone tacks or bone screws over exposed bone at a desired bone graft site in the alveolar ridge of a patient such that the membrane defines a space having a predetermined height and width over the exposed bone, in which the membrane maintains its structural integrity for at least 4 months after implantation at the bone graft site and then naturally breaks down and is resorbed by the patient's body, a method of making such a membrane, and a method of using such a membrane for vertical augmentation of the alveolar ridge of the patient.

A bone repair material is described that is of putty-like consistency, particularly useful for repairing dental bony defects such as those caused by bone loss resulting from moderate or severe periodontitis, augmenting of bony defects of the alveolar ridge, filling tooth extraction sites, or sinus elevation grafting. The repair material includes a porous, resorbable particulate that is bone-derived or derived from bone-like hydroxyapatite or synthetic hydroxyapatite; and, a resorbable carrier, such as high molecular weight polysaccharides, such as hyaluronic acid. A high concentration of particulate in the putty enhances bone repair and requires a high concentration of carrier to retain the putty at the defect site. For a particulate density of about 1.2 g / cc such as PEPGEN P-15® Bone Graft, a preferred formulation comprises about 55% percent by weight of the putty suspended in a hyaluronic acid gel of about 1.4×106 daltons molecular weight and a final concentration of about 56 mg / cc which material adheres to a bony periodontal defect and does not excessively expand or migrate from the defect when held in place by a conventional flap closure.