A medical or dental, hand-held treatment instrument, comprising a single-part or multi-part outer sleeve, at least one controlling element having at least one capacitive sensor and a sensor surface provided on the outer sleeve and operatively connected to the capacitive sensor, wherein the controlling element generates an actuating signal when the sensor surface is touched or approached. The treatment instrument further comprises an indicating device, which is arranged on the treatment instrument and which indicates the sensor surface and/or the generation of an actuating signal due to a contact of the sensor surface or an approach to the sensor surface.

A suture device comprises at least one weft strand interwoven with a plurality of warp strands to define a body region. The body region has a substantially open mesh construction and at least a first elongate end region axially extending from and being one part with the body region having a substantially closed mesh construction. The width of the end region is substantially less than a width of the body region.

The present invention relates to a compression aid for compressing a puncture site of a patient, wherein the compression aid comprises a peripheral band whose circumference can be adjusted, with a constant force spring being arranged in the peripheral band.

Surgical instruments are disclosed comprising a firing assembly including a fuse having a plurality of operating states.

A container holds at least one surgical implement, has a lock mechanism, and has a signature label that impedes access to the surgical implement until the correct surgical site is confirmed. A method of using the container includes the steps of confirming the correct surgical site, signing the label and removing it from the container, placing the label in the medical record, unlocking the container, removing the implement, and beginning the surgery, wherein the surgical team is forced to pause to confirm the correct surgical site before starting the surgery. The system and method may also include a wrong site surgery profile used by individuals within the surgical procedure environment and third parties for tracking and determining if, and where, a wrong site surgical procedure occurred. The profile can be updated, tacked and monitored while a patient is interacting within the medical environment.

A method of dispensing surgical fasteners includes providing an applicator instrument having a housing with a cartridge opening, an elongated shaft extending from the housing, a firing system disposed within the housing for dispensing surgical fasteners, and an actuator for activating the firing system. The method includes forming a surgical opening in tissue, inserting a distal end of the elongated shaft into the surgical opening, inserting a cartridge containing a plurality of first surgical fasteners into the cartridge opening, and engaging the actuator for dispensing one of the first surgical fasteners from the distal end of the elongated shaft. While maintaining the distal end of the elongated shaft inside the surgical opening, the cartridge is removed from the cartridge opening, a second cartridge containing a plurality of second surgical fasteners is inserted into the cartridge opening, and the actuator is engaged for dispensing one of the second surgical fasteners from the distal end of the elongated shaft.

A suture construct that is elongate along a longitudinal direction and configured to change in size from a first configuration to a second configuration includes an outer layer of material that extends along the longitudinal direction and has a plurality of intertwined fibers that comprise a first sub-set of fibers crossed by a second sub-set of fibers at respective intersections, such that the first subset of fibers and the second subset of fibers are configured to reorient relative to each other in a manner causing the outer layer of material to change in one or more of surface texture and visual appearance as the suture construct changes between the first and second configurations.

In various embodiments, a tissue thickness compensator can comprise a compressible extracellular matrix and a bioabsorbable material dispersed within the extracellular matrix, wherein the bioapsorption of the bioabsorbable material is configured to leave behind channels in the extracellular matrix. The tissue thickness compensator can also comprise generation means for generating the ingrowth of tissue into the channels. In at least one embodiment, the tissue thickness compensator can comprise dissolvable wicking members which, when dissolved, can leave behind channels in the tissue thickness compensator. In certain embodiments, the tissue thickness compensator can comprise at least one rupturable capsule.

In various embodiments, a tissue thickness compensator can comprise a compressible extracellular matrix and a bioabsorbable material dispersed within the extracellular matrix, wherein the bioapsorption of the bioabsorbable material is configured to leave behind channels in the extracellular matrix. The tissue thickness compensator can also comprise generation means for generating the ingrowth of tissue into the channels. In at least one embodiment, the tissue thickness compensator can comprise dissolvable wicking members which, when dissolved, can leave behind channels in the tissue thickness compensator. In certain embodiments, the tissue thickness compensator can comprise at least one rupturable capsule.

A suture includes an outer sheath with color marks and a background visually distinguishable from the color marks. Each color mark has exposed portions of at least two colored yarns of first and second different colors. The background includes exposed portions of background yarns of a background color. The background yarns and the colored yarns are braided to each other. The first and second colors are different from the background color. The color marks are arranged in at least one row along a longitudinal direction of the suture. Each color mark is longitudinally shifted with respect to a subsequent color mark in a same row by a first shift, and the exposed portions of the colored yarns of each color mark are substantially parallel to each other and arranged in a sequence along the longitudinal direction of the suture.