Abstract: A saliva control device for controlling saliva flow from a salivary duct without damaging the salivary duct and surrounding soft oral tissue includes an elastic body, a constriction hole formed through the elastic body, and an interior wall defining the constriction hole. The interior wall is substantially smooth and the elastic body sufficiently stretchable that the constriction hole expands during placement around a salivary duct and the wall constricts around the salivary duct to prevent flow of saliva without substantially cutting off blood flow to and damaging the salivary duct and soft oral tissue surrounding the salivary duct.

Abstract: A plunger-barrel apparatus is adapted for use within a syringe-in-syringe mixing system for mixing a two-part composition (e.g., a dental composition). A hollow plunger-barrel body has a continuous cylindrical wall defining an internal chamber for containing a first component. The body includes a plunger receiving end and a dispensing end. An integral sealing plug and rupturable membrane is disposed at the dispensing end of the body and include a sealing plug portion and a rupturable membrane portion that are integrally formed together as a single piece (e.g., formed of a single piece of elastomeric material). An associated syringe-in-syringe mixing system includes a first plunger, the hollow plunger-barrel body as described above adapted to contain a first component, and a syringe barrel configured to contain a second component. When assembled, the first plunger is slidably disposed within the hollow plunger-barrel body, and the plunger-barrel body is slidably disposed within the syringe barrel.

Abstract: Kits and methods facilitate chair-side coating of an endodontic cone for improved sealing between the hydrophilic root canal tissue, the hydrophobic elastomer substrate of the endodontic cone, and a hydrophilic sealing resin. The kit includes one or more endodontic cones (e.g., formed of gutta percha) and a micro-dose container containing an adhesive composition. The practitioner can dip the cones into the adhesive composition so as to coat the cones chair-side, just prior to use. The adhesive composition includes an adhesive resin compound comprising at least one hydrophobic region and at least one hydrophilic region. The hydrophobic region is compatible with the hydrophobic elastomer substrate of the endodontic cone, while the hydrophilic region is compatible with a hydrophilic endodontic sealing resin.

Abstract: Activating endodontic points and dental tools are sized and configured to be placed in the root canal of a tooth. The activating endodontic points or dental tools are coated or impregnated with a curing agent that initiates or accelerates polymerization of a sealer or filling composition when placed in contact with the sealer or filler material. Curing agents can include amines that can destabilize a peroxide in the sealer or filler material to initiate or accelerate polymerization. Kits are also disclosed that include a plurality of endodontic points or dental tools that have different concentrations of curing agent coated on or impregnated within the endodontic points or dental tools such that the endodontic points or dental tools have different cure times. In another kit, a plurality of curing agent compositions are provided for dipping a substrate to coat or impregnate substrates having different concentrations of curing agent.

Abstract: An anti-microbial and/or anti-viral composition for use in disinfecting an oral tissue during a dental procedure includes at least one dental operative material that is allowed to contact the oral tissue for a period of time between about 2 seconds and about 1 month and an effective amount of an anti-viral and/or anti-bacterial agent included in or mixed with the dental operative material so as to impart an anti-bacterial and/or anti-viral effect at or near a site of administration in oral tissue. The anti-viral and/or anti-bacterial agent at least partially at least partially contributes to a two-log (or three-log, four-log, or five-log) reduction in viral and/or bacterial activity at or near a site of administration. The compositions protect a dental practitioner and/or other patient from being infected by a communicable disease carried by a treated patient.

Abstract: A pre-dosed, pre-packaged mixing system and associated method for mixing, storing, and dispensing a two-part dental composition that becomes less stable upon mixing. The mixing system includes a pre-dosed, pre-packaged quantity of a first component contained within a first chamber, and a pre-dosed, pre-packaged quantity of a second component contained within a second chamber. The chambers are separated by separation means so as to separate the two-components prior to mixing. Once mixed, the practitioner is able to record a mixing and/or expiration date on at least a portion of the mixing system so as to indicate a shelf-life of the less stable mixed dental composition.

Abstract: A root canal is filled and/or sealed using a hydrophilic sealing composition, optionally in combination with other filling materials. The sealing composition may include one or more resins that promote adhesion to hydrophilic dental tissues. The composition may be introduced into the root canal using a narrow cannula coupled to a high pressure hydraulic delivery device. In the case where a chemical cure composition is used to seal the root canal, a chemical initiator can be used to cause the mixed composition to harden over time. Hardening of at least a portion of the composition can be accelerated by including a photoinitiator and irratiating the mixed composition with radiant energy (e.g., from a dental curing lamp).

Abstract: A hollow inner plunger for use within a syringe-in-syringe mixing system for mixing a two-part dental composition. The hollow inner plunger includes a body having a continuous cylindrical wall defining an internal chamber for containing a first component. The body includes a proximal end and a distal end. A sealing plug and rupturable membrane are disposed at the distal end of the body, and the sealing plug and rupturable membrane are integrally formed together as a single piece (e.g., formed of a single piece of elastomeric material). An associated syringe-in-syringe mixing system includes a first plunger, the hollow inner plunger as described above, and a syringe barrel configured to contain a second component. When assembled, the first plunger is slidably disposed within the hollow inner plunger, and the hollow inner plunger is slidably disposed within the syringe barrel. The two components are initially separated by the rupturable membrane.

Abstract: Endodontic instruments or intermediate products (e.g., blanks) used to form finished endodontic instruments having a desired cutting edge and/or taper are formed, at least in part, by molding a metal powder into a desired shape and then sintering the metal particles together. The metal powder is initially formed into a green molded part that is sintered to yield a solid metal part. The sintered metal part may optionally be further processed by additional steps, as needed, to yield a finished endodontic instrument. One additional process includes cold forming the sintered metal body to provide a cutting edge, remove cracks and microfissures, or otherwise modify the characteristics of an intermediate product or endodontic instrument. Other processes include chemical milling and mechanical milling, grinding or cutting to sharpen the cutting edge, form a taper, or otherwise modify the intermediate product or endodontic instrument in a desired manner.

Abstract: A brush tipped applicator includes an applicator tip having a body defining an external surface and an internal conduit. The applicator tip body can have a proximal end defining a proximal opening of the internal conduit and a distal end. The proximal end of the applicator tip body can have a first fastener that is configured for being coupled to a fastener (i.e., second fastener) of a member containing the dental bleaching composition such that the internal conduit of the applicator tip body is capable of being fluidly coupled with the dental bleaching composition. Additionally, the brush tip includes at least one filament disposed on the external surface of the applicator tip body. A dental bleach activator disposed within the filament in an amount sufficient for activating the dental bleaching composition for whitening the teeth.

Abstract: An adapter for use with an air/water tip (e.g., a three-way dental syringe). The adapter comprises a body including a proximal end and a distal end, a mixing chamber disposed between the proximal and distal ends, a water delivery lumen for delivering water from a coupleable fluid dispensing device to the mixing chamber, and a separate air delivery lumen for delivering air from a coupleable fluid dispensing device to the mixing chamber. The cross-sectional area of the water delivery lumen at a location adjacent the mixing chamber is greater than the cross-sectional area of the air delivery lumen at a location adjacent the mixing chamber. The relative cross-sectional areas act to balance pressures of air and water entering the mixing chamber so as to provide a ratio of volumetric flow rate of water to air that is between about 0.5:1 to about 2:1.

Abstract: Non-customized dental treatment trays used to provide a desired treatment are formed from elastomeric silicone or silicone-like material. They may be injection molded from a two-part liquid silicone composition or a silicone-like TPE material (e.g., preferably SEBS and/or VERSAflex thermoplastic elastomer). The dental treatment trays possess high adaptability, flexibility, softness, and elastic elongation while also exhibiting resiliency in order to readily conform to the ridges, depressions and contours of a person's teeth during use. The trays possess a greater ability to adhere to a person's teeth compared to non-elastomeric thermoplastic materials. Due to their high adaptability and conformability, the non-customized dental trays behave like a semi-custom dental tray when placed over conformed to a person's teeth, particularly when used in combination with a sticky, viscous treatment composition.

Abstract: Endodontic instruments having a desired cutting edge are formed, at least in part, using a cold forming process. The method of forming the endodontic instrument includes providing a blank metal thread or wire and at least one die that has a negative impression of a cutting edge. The die is pressed against the blank with sufficient force in order for the die to form an at least partially formed cutting edge in the blank. Any desired shape can be formed into the blank by selecting a die with the proper corresponding negative impression. Cold forming techniques suitable for forming endodontic instruments include roll forming, flat rolling, radial forming, cold drawing, and similar techniques. The files can be sharpened or otherwise modified before or after cold-forming using techniques such as cutting, grinding, and chemical milling.

Abstract: Methods and associated kits for use in selectively conditioning and remineralizing teeth. An exemplary method comprises the steps of applying a conditioning composition to one or more of a person's teeth, and applying a remineralizing composition to the person's teeth. The conditioning composition includes a conditioning agent, and the remineralizing composition includes a remineralizing agent comprising calcium ions and/or fluoride ions. The conditioning composition may be applied prior to or after application of the remineralizing composition. In one embodiment, both the conditioning composition and the remineralizing composition include different remineralizing ions (e.g., one including calcium, one including fluoride).

Abstract: Dental treatment trays and strips used to deliver a dental bleaching composition to a person's teeth are formed from a moisture resistant barrier material and include a bleaching agent destabilizer disposed on an inner treatment surface of the barrier layer that is positioned against the person's teeth during use. The bleaching agent destabilizer may be compounded with the moisture resistant material or otherwise disposed relative to the barrier layer so that at least some destabilizer is positioned on the inner treatment surface of the tray or strip so as to contact the dental bleaching composition during use.

Abstract: Self-ligating orthodontic brackets include a bracket base, at least one arch wire slot formed in the bracket base adapted to receive an arch wire therein, and a ligation cover which is selectively slidable relative to the bracket base between an open non-ligating position relative to the slot and a closed, ligating position relative to the slot. The exterior labial surface of both the base and ligation cover comprise a compound two axis curvature so that substantially all of the exterior labial surface of both the bracket base and the ligation cover present a smooth, continuous exterior surface that is substantially free of sharp discontinuities and crevices.

Abstract: Orthodontic brackets having a bracket base including at least one arch wire slot formed therein and a bendable or flexible member (e.g., a film hinge) having a relatively thin cross-sectional thickness to facilitate flexing or bending of the member with little or no permanent deformation, wherein at least the bendable or flexible member comprises an amorphous metallic alloy.

Abstract: Apparatus assemblies and methods for melting and injection molding an article from a meltable metal that is sensitive to heating by radio frequency (RF) induction. An exemplary apparatus includes a mold including a cavity having a shape of an article to be molded, a delivery chute including a channel for delivering a solid metal billet from a proximal end of the delivery chute to a distal end which is adjacent to the mold, and an RF induction heating coil that surrounds the cavity of the mold and the distal end of the delivery chute. Advantageously, the portion of the mold defining the cavity and at least the distal end of the delivery chute (i.e., those portions surrounded by the RF coil) are formed of materials that are substantially insensitive to heating by RF induction so that the metal billet is melted and molded at approximately the same time.

Abstract: A degradation resistant gingival retraction cord comprising or consisting essentially of silk is formed from two or more strands that are braided, twisted or woven. The degradation resistant retraction cord comprises at least about 50% silk, 80% silk, 90% silk, 95% silk, or essentially all silk. They are able to maintain at least about 70%, 80% or 90% of this tensile strength for a time period of at least about 7 days, 30 days, 60 days, or 90 days. The silk retraction cords have the look, feel and desirable utility of a thin, flexible, and resilient natural fiber cord, while also resisting degradation when pre-impregnated with a corrosive agent. Such cords combine the degradation resistance of a man-made fiber, while also having greater liquid absorbance, lightness, flexibility and resilience like a natural fiber cord.

Abstract: Treatment devices in the shape of a dental tray, strip or patch include a barrier layer and a protective adhesive composition. Treatment kits include one or more treatment devices and one or more treatment compositions that are initially separate from the treatment devices. The treatment compositions may be contained within a syringe (e.g., a unit dose syringe) for ease of delivery. The treatment composition is dispensed from the syringe onto the barrier layer and then placed over a person's teeth and/or gums. The protective adhesive composition, in combination with the barrier layer, at least partially confines the treatment composition to a desired location within the person's mouth during use. The barrier layer protects the treatment and protective adhesive compositions from saliva or moisture found in the person's mouth.