The invention relates to a medical implant (1) that is adapted to repair or close defect (D), in particular an opening in a ventricular, atrial, or septal wall (W). The medical implant (1) may, in particular, be a patch. It comprises an adhesive composition (6). It further comprises two states, wherein in the first state, the medical implant (1) can be deployed to an implant site while the adhesive composition (6) is inactive. It can be brought into a second state by an activation mechanism. The adhesive composition (6), in the second state, is curable by a curing mechanism.

A surgical guide and methods of using the surgical guide are disclosed. The surgical guide includes a body having a first side and a second side. An adhesive material is disposed over at least a portion of the first side. A radiopaque guide element coupled to a second side of the body and an incision guard defines an opening extending from the first side to the second side of the body. The incision guard is sized and configured to receive a surgical instrument therethrough such that the incision guard prevents contact between the surgical instrument and a portion of a surgical site adjacent to the opening.

In general, systems and methods described herein include active or passive sensing mechanisms, such as sensors, that can monitor at least one exposure condition of an adjunct and any medicant(s) retained therein. In some instances, the active or passive sensing mechanisms can also track the extent of the adjunct's and medicant(s)'s exposure, e.g., frequency, intensity, and/or duration).

In general, systems and methods described herein include active or passive sensing mechanisms, such as sensors, that can monitor at least one exposure condition of an adjunct and any medicant(s) retained therein. In some instances, the active or passive sensing mechanisms can also track the extent of the adjunct's and medicant(s)'s exposure, e.g., frequency, intensity, and/or duration).

In general, systems and methods described herein include active or passive sensing mechanisms, such as sensors, that can monitor at least one exposure condition of an adjunct and any medicant(s) retained therein. In some instances, the active or passive sensing mechanisms can also track the extent of the adjunct's and medicant(s)'s exposure, e.g., frequency, intensity, and/or duration).

Compressible adjuncts for use with a staple cartridge are provided. In one exemplary embodiment, the compressible adjunct includes a non-fibrous adjunct material formed of at least one fused bioabsorbable polymer. The adjunct material is configured to be releasably retained on a staple cartridge and is configured to be delivered to tissue by deployment of staples in the cartridge The adjunct material includes a lattice macrostructure having at least one drug contained therein. The lattice macrostructure is formed of a plurality of unit cells, in which each unit cell is configured to eject a predetermined amount of drug from the adjunct material and the predetermined amount of the drug being a function of a compression profile of the respective unit cell.

An instrument for isolating candidate eyelashes to attach prostheses includes an instrument tip which has a tip aperture. A candidate eyelash is disposed in a distal slot of the tip aperture. The instrument tip is advanced relative to the candidate eyelash and the instrument tip applies a force to eyelashes that are adjacent to the candidate eyelash. The application of the force actuates the eyelashes that are adjacent to the candidate eyelash away from the candidate eyelash. The candidate eyelash is actuated into an open area of the tip aperture and a prosthesis is attached to the candidate eyelash.

A method for constructing a braided implant delivery system and treating an aneurysm can include attaching a braided implant having a band attached thereto to a delivery tube, positioning the braided implant within the aneurysm, and releasing the band from the delivery tube, thereby releasing the braided implant. The band can include movable extensions that can press into an outer surface of the delivery tube to secure the band to the delivery tube then move away from the outer surface of the delivery tube to release the band. A pull wire can be engaged to the band to secure the band to the delivery tube then be pulled proximally to release the band from the delivery tube. At least a portion of the braid of the braided implant can be positioned within a lumen of the delivery tube.

A treatment energy application structure includes a flexible substrate having an electric resistance pattern and a lead wire connection portion. A heat transfer plate faces the flexible substrate and transfers heat to the body tissue. An insulating adhesive sheet is interposed between the flexible substrate and the heat transfer plate. The insulating adhesive sheet comprises a first area to cover an entire surface of the electric resistance pattern and the heat transfer plate and a second area protruding from the heat transfer plate to cover a part of the lead wire connection portion. The heat transfer plate has a chamfered corner facing the insulating adhesive sheet. An adhesive may adhere the second area to at least one of the heat transfer plate and the substrate. The insulating adhesive sheet may adhere the substrate to both the heat transfer plate and the bridge portion of a cover.

The present invention provides an anchor system for musculoskeletal applications, e.g., for anchoring tendons or ligaments to bone or anchoring two or more bone sections. The anchor system comprises a substantially solid pre-manufactured distal portion (i.e., anchor component) and a settable, biodegradable composite. The biodegradable composite is flowable at the time of delivery and is introduced into the fixation site before or after the anchor component. Both the anchor component and the biodegradable composite may be manufactured from citrate-based polymers.