A combination includes a dental handpiece and a prophy angle. The dental handpiece includes a nosecone threadably connected to the dental handpiece. The prophy angle includes a proximal body that matingly attaches to the nosecone. A plurality of elongated torque members are formed on each of the prophy angle proximal body and the nosecone. Each of the torque members is a male torque member or a female torque member and each male torque member formed on one of the prophy angle proximal body and the nosecone matingly couples with a female torque member formed on the other of the nosecone and the prophy angle proximal body. The prophy angle, including the plurality of elongated torque members formed on the prophy angle, is formed to also be attachable to a known standard doriot-style nosecone. Other specific features of the handpiece and prophy angle are also disclosed.

A dental system comprises a dental prophy angle and an adjustable angle adapter. The prophy angle includes a housing and a guard with a concave inner surface. The adapter is configured to drive the prophy angle and the adapter includes a body, a nose, and an outer joint. The nose is configured to receive a portion of a prophy angle. The body is adjustably connected to the nose. The outer joint includes a ball portion connected to the nose, and a ball receiver positioned on the body. The ball receiver includes a first portion coupled to a first end of the body and a second portion attachable to the first portion. The nose is rotatable relative to the body into at least a first configuration and a second configuration. The concave inner surface of the guard engages a convex outer surface of the ball receiver.

The invention relates to a dental tool having a shank region, which is formed for coupling to a dental handpiece, and also having a work region, which is connected to the shank region. In this case, the shank region of the dental tool is formed so that there is the possibility of latchable insertion and removal without actuation. In particular, at least the shank region can consist of plastics material. As a result, inter alia facilitated handling of the tool and inexpensive production of the tool are rendered possible.

An oral health care implement and system are provided for use during oral health care activities. The oral health care implement has an oximetry sensor, most often in the embodiment of a transmissive or reflective pulse oximeter. The oximetry sensor provides blood oxygen saturation and heart rate measurements. The oral health care system has an oral health care implement, a first data transfer medium, and any combination of: a second data transfer medium, a network storage device, and a third data transfer medium. The system provides means for collecting a user's vital signs and transmitting data into a readable, usable form for the user via an oral health care implement.

An oral health care implement and system are provided for use during oral health care activities. The oral health care implement has an oximetry sensor, most often in the embodiment of a transmissive or reflective pulse oximeter. The oximetry sensor provides blood oxygen saturation and heart rate measurements. The oral health care system has an oral health care implement, a first data transfer medium, and any combination of: a second data transfer medium, a network storage device, and a third data transfer medium. The system provides means for collecting a user's vital signs and transmitting data into a readable, usable form for the user via an oral health care implement.

There is a need for a minimally invasive surgical treatment method for periodontitis for the removal of deep pockets, elimination of disease, creation of reattachment of the gingiva to the tooth surface and true regeneration of the attachment apparatus (new cementum, new periodontal ligament, and new alveolar bone) on a previously diseased root surface. The PerioLase® MVP-7™ including eGUI or another device capable of laser dosimetry, such as an original MVP-7™ type laser without the eGUI, achieves this with the LANAP protocol (laser-assisted new attachment procedure) and the LENAP protocol (laser excisional new attachment procedure).

Described herein are systems and methods for providing personalized oral irrigation. One variation of a system for personalized oral irrigation comprises a fluid reservoir and a customized oral insert in fluid communication with the fluid reservoir. The oral insert comprises an arrangement of fluid openings positioned based on the individual oral or dental structures of a user's teeth to provide a customized fluid flow over the user's teeth. Also described herein are methods for generating an arrangement of fluid openings in a customized oral insert.

Described herein are systems and methods for providing personalized oral irrigation. One variation of a system for personalized oral irrigation comprises a fluid reservoir and a customized oral insert in fluid communication with the fluid reservoir. The oral insert comprises an arrangement of fluid openings positioned based on the individual oral or dental structures of a user's teeth to provide a customized fluid flow over the user's teeth. Also described herein are methods for generating an arrangement of fluid openings in a customized oral insert.

A cannula for a multifunction dental syringe includes a fastener bushing that is defined by a circular opening, an end wall, and a side wall comprising a circular cylinder. The cannula also includes at least two channels enabling fluids to be conveyed separately or together from the end wall to fluid projection orifices, and beginning in the end wall beside each other. The cannula is arranged so that the circular cylinder presents a cutout in the thickness of its wall. The cutout comprises, going from the opening, at least one segment extending in a direction other than the axial direction of the cylinder; followed by a longitudinal segment extending towards the end wall.

A cannula for a multifunction dental syringe includes a fastener bushing that is defined by a circular opening, an end wall, and a side wall comprising a circular cylinder. The cannula also includes at least two channels enabling fluids to be conveyed separately or together from the end wall to fluid projection orifices, and beginning in the end wall beside each other. The cannula is arranged so that the circular cylinder presents a cutout in the thickness of its wall. The cutout comprises, going from the opening, at least one segment extending in a direction other than the axial direction of the cylinder; followed by a longitudinal segment extending towards the end wall.