52 results about "Extraction site" patented technology

Methods and apparatus are presented for extracting and collecting bone material from an extraction site of a patient. The method and apparatus further provides a readily accessible, and easily harvested, source of bone material without the drawbacks of current extraction methods.

A detachable electrode and anchor utilized with electrode leads and leadless medical implants that enable explantation of the electrode while leaving the anchor in place. The detachable electrode and anchor utilizes a detachable mechanism that detachably couples the electrode to the anchor. Embodiments do not require removal of existing scar tissue before explantation, which minimize chances of internal bleeding at the extraction site. Embodiments also minimize impact on the vein in which the electrode lead travels by eliminating use of a necessarily larger diameter sheath that is utilized around the electrode lead to remove the electrode lead and attached anchor.

A moldable, bioresorbable, biocompatible, non-allergenic crosslinked collagen derivative dressing for the prevention of post extraction alveolar osteitis (dry socket) pain is disclosed along with methods for use of the gel. The dressing is placed at the time of surgery acting as a bone covering obtundant and physiologic scaffolding for the conduction of normal alveolar bone healing sequence of fibroblast ingrowth, blood vessel formation, and reossification of the extraction site defect. In one form, the dressing is a flowable, moldable, biocompatible, bioresorbable dressing prepared by reacting (i) a collagen derivative, such as gelatin or atelocollagen, and (ii) a non-cytotoxic crosslinking agent.

The present invention uses an anatomically shaped bone graft contouring abutment in place of a conventional healing abutment to control the bone graft for optimal height. The extraction site aesthetics, in the form of enhanced gingival growth, are facilitated by the optimal bone graft placement.

The present invention uses an anatomically shaped bone graft contouring abutment in place of a conventional healing abutment to control the bone graft for optimal height. The extraction site aesthetics, in the form of enhanced gingival growth, are facilitated by the optimal bone graft placement.

A submergible or non-submergible (“one stage”) screw-type implant for use in the immediate post-extraction site of a patient's tooth. In order to increase the ability of regenerated bone to anchor the implant, an upper portion of the implant has a preferably generally conical shape and has a plurality of spherical projections sintered to its outer surface to make it suitable for bone integration and retention. The lower portion of the implant has a cylindrical shape with threads extending over a portion thereof. A channel is located through the threads and is shaped so that one side forms a cutting edge that makes the lower portion of the implant self-tapping into the bone at the base of the tooth extension socket.

The invention relates to a method for evaluating efficacy of an antler, which takes the bifidobacterium in a gastrointestinal tract as representative of beneficial bacterium and takes staphylococcus as representative of harmful bacterium.The method objectively and quantitatively evaluates the influence of different extraction sites of antler alcohol extract on the growth and metabolism of microorganism in the gastrointestinal tract through obtaining a thermogram and other comprehensive information which can fully reflect the interaction process and has overall expression characteristics, screens the active site with the strongest bacterium-promoting action of the antler and inspects the bacteriostasis of the active side simultaneously. The method has simple operation, easy standardization and automation of the detection.

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.

Embodiments are directed to managing and improving a drilling and completions process at a hydrocarbon extraction site, and to optimizing resource allocation at a hydrocarbon extraction site / region. In one scenario, a computer system accesses data generated by hardware sensors implemented by drilling and completion equipment at a hydrocarbon extraction site. The computer system formats the sensor data into a form readable by a data mining algorithm, and mines the formatted sensor data to identify characteristics related to the drilling and completion process. The computer system also accesses and integrates historical data related to the drilling and completion equipment at the hydrocarbon extraction site. The computer system then computes drilling and completion performance indicators that identify inefficiencies based on the characteristics identified for the equipment and based on the accessed historical data. Then, a remediation step is performed to resolve the identified inefficiency.

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.

A method for increasing the distance between outer surface of tissue proximate to a surgical extraction site and a patient's sensitive body tissues comprising the infusion of a solution at a location of minimum distance between the extraction site and the sensitive body tissue until the accumulation of fluid distends the sensitive body tissue away from the extraction site.

Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The goal of the pellets are to encourage sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

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.

Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The goal of the pellets are to encourage sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

The extraction socket devices are designed to protect the extraction socket immediately after tooth extraction. These devices protect the socket from oral bacteria and food, support a space to prevent collapse of the alveolar ridge during healing, contain any bone graft material inside of the socket, and provide comfort to patient during the healing process. Procedures are also disclosed for placing the devices in an extraction site to obtain the benefits of the disclosed devices.

A dispenser provided by a dispenser body with an article storage chamber bounded by at least one panel with an article extraction site leading to an article storage chamber containing at least one stack of articles folded over at least once in a non-binding arrangement with each article in the stack oriented in the same direction and with the outermost article disposed proximate the extraction site and constructed to slide off the folded article stack and out through the extraction site while leaving the next article in the folded article stack exposed for subsequent withdrawal wherein the articles may be selectively withdrawn one at a time through the extraction site until the innermost article is removed from the article storage chamber along with methods of loading and dispensing such dispensers are described herein.

A dispenser that may be loaded with a plurality of interconnected articles with at least one grasping section and that may then be selectively withdrawn one at a time out through an extraction site and indexed for subsequent withdrawal upon removal along with methods of manufacturing and assembling, the article itself, and additional features such as a separator for engaging the article to dispense the article in an open configuration, a restrainer for aiding separation of the articles, and an elevator or ramp for locating the grasping sections of the articles near the extraction site are disclosed herein.

Various embodiments include methods and apparatuses of forming turbomachine casing intermediate structures. In some embodiments apparatuses include a steam turbomachine casing intermediate structure including an inner shell having an external surface and inner shell cavity, and defining an opening for allowing fluid entry to the cavity and an outer shell having an internal surface, these surfaces defining at least one closed, axial-extending chamber, the inner shell and outer shells each having access regions adjacent the closed chamber, each of the access regions including a plurality of locations, selectable to be machined to create an exhaust slot or an exhaust opening in the inner casing or the outer casing, respectively, and wherein a structural integrity of the casing is uniform regardless of which of the axial locations are selected to be machined, where the exhaust opening is fluidly connected with the at least one closed chamber through the outer shell.

A dispenser that may be loaded with a plurality of interconnected articles with at least one grasping section and that may then be selectively withdrawn one at a time out through an extraction site and indexed for subsequent withdrawal upon removal along with methods of manufacturing and assembling, the article itself, and additional features such as a separator for engaging the article to dispense the article in an open configuration, a restrainer for aiding separation of the articles, and an elevator or ramp for locating the grasping sections of the articles near the extraction site are disclosed herein.

Embodiments of the present disclosure are directed to apparatuses and methods for pre-conditioning an extraction site for dental implantation. In one implementation, a method for pre-conditioning an extraction site for dental implantation includes providing a vibrational dental device configured to vibrate at a frequency higher than about 20 Hz. The method further includes providing instructions for mechanically vibrating, using the vibrational dental device, a tooth at the extraction site for about a predetermined period of time daily over a treatment period before extracting the tooth. The mechanical vibration may prepare the extraction site to be in a healthier condition for receiving an implant.

Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The goal of the pellets are to encourage sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

The invention relates to a Cordyceps sobolifera active site and application thereof in preparing drugs for nerve protection and aging resistance. The active site is a Cordyceps sobolifera alcohol extract ethyl acetate extraction site. The active site is prepared by the following steps: pulverizing the medicinal material Cordyceps sobolifera, screening, extracting with ethanol under reflux, dispersing the ethanol extract with water, sequentially carrying out fractional extraction with petroleum ether, ethyl acetate and n-butanol for 3-5 times, merging, concentrating under reduced pressure to recover the solvent, and carrying out freeze-drying to respectively obtain a petroleum ether site, an ethyl acetate site, an n-butanol site and a water site. The ethyl acetate site can obviously inhibit aging and damage of the glutamic-acid-induced PC12 cells, prevent the cell LDH from release, enhance the survival rate of the cells, lower the intracellular oxygen free radical level, enhance the activity of the glutathione reductase (GSH-Px) and superoxide dismutase (SOD), and have favorable in-vitro oxidation resistance activity in the experiment of clearing DPPH. and superoxide anion (O<2.->) free radicals.

There is disclosed a waste treatment process for a fossil-fuel extraction site (18, 40), comprising: processing extracted waste generated by a fossil-fuel extraction process to produce primary waste having a higher calorific value than the extracted waste; mixing the primary waste with secondary waste to generate pyrolysis feedstock, the secondary waste having a lower calorific value than the primary waste; pyrolysing the pyrolysis feedstock in a pyrolysis unit (32) to form pyrolysis char; and gasifying the pyrolysis char in a gasification unit (36) to form syngas and ash.

The present invention provides an oil extraction site safety monitoring device. The device comprises an oil well device monitoring unit, an oil gas transmission monitoring unit, a concentration control unit and a remote server. The oil well device monitoring unit comprises a device communication monitoring module, and the signal monitoring device comprises a signal monitor on a line. The oil gas transmission monitoring unit performs real-time monitoring of the oil gas conveying line, and the oil gas transmission monitoring unit comprises a transmission operation monitoring module. The oil gas transmission unit comprises a transmission environment monitoring module. The oil well device monitoring unit comprises a transmission communication monitoring module. The oil extraction site safety monitoring device is provided with multi-group sensors to perform real-time monitoring of the operation, the environment and the communication so as to ensure the normal operation of the oil extraction and transmission, the wearing of the device is reduced in the operation process, the repairing is timely performed, and the service life of the device is prolonged; and the bad phenomenon of the occurrence of forcing to stop and other severe damaging is avoided so as to greatly reduce the potential safety hazard and improve the safety performance.

The invention discloses a delivery monitoring method and device, and relates to the technical field of computers. A specific implementation of the method includes: collecting multiple frames of images in a designated area, identifying the delivery site of the target object in the multiple frames of images, determining the location of the delivery site, and extracting the delivery site image; according to a predetermined slice processing method, Perform slice processing on the delivery site image to obtain color picture slices and frame difference picture slices; input the color picture slices and frame difference picture slices into the predetermined behavior recognition network to obtain the delivery stage of the target object. In this implementation mode, only the delivery site of the target object to be delivered is monitored to reduce the interference of unnecessary factors; the traditional 3DCNN network is improved, the input of video frame difference is increased, and the robustness of the overall method is greatly improved , the overall replacement of the existing artificial care, reducing the cost of input.

The invention provides a sample extraction device for biochemical testing, which includes a protective pad, a fixed cylinder, an extraction device, and a handle. The protective pad is installed on the lower part of the fixed cylinder; the extraction device is installed inside the fixed cylinder; the The handle is installed on the upper part of the fixed cylinder. The setting of the ball screw of the present invention, the color liquid crystal display screen and the protective pad is convenient to the control of the downward position, the observation of the extracted part is convenient, the situation of the extracted part is known in time, the cleanliness of the extracted part is ensured, and the risk of infection is avoided. occur.