The present disclosure relates to various anchoring assemblies, systems, and methods for a catheter delivered device or otherwise implantable biomedical sensors. In one instance the anchoring systems of the present disclosure are designed to be used in connection with a biomedical sensor configured to be placed in the various locations within the anatomy of a patient including: a junction of a renal vein and an inferior vena cava, a junction of a jugular vein branch and a subclavian vein branch, a junction of a brachiocephalic vein branch and a superior vena cava, or a junction of an iliac vein branch and an inferior vena cava. In one embodiment, an biomedical sensor and anchoring system can be implanted in an organ of a patient or in an organ to be transplanted within a patient.

A method for monitoring a cardiovascular pressure in a patient includes measuring, by pressure sensing circuitry of an implantable pressure sensing device, the cardiovascular pressure of the patient. The method further includes transmitting, via wireless communication circuitry of the implantable pressure sensing device, the measured cardiovascular pressure to another device. The method further includes determining, by processing circuitry of the other device, whether a posture of the patient at a time of the measured cardiovascular pressure was a target posture for cardiovascular pressure measurements. The method further includes determining, by the processing circuitry of the other device, whether to store or discard the transmitted cardiovascular pressure based on determining whether the posture was the target posture.

A method for monitoring a cardiovascular pressure in a patient includes measuring, by pressure sensing circuitry of an implantable pressure sensing device, the cardiovascular pressure of the patient. The method further includes transmitting, via wireless communication circuitry of the implantable pressure sensing device, the measured cardiovascular pressure to another device. The method further includes determining, by processing circuitry of the other device, whether a posture of the patient at a time of the measured cardiovascular pressure was a target posture for cardiovascular pressure measurements. The method further includes determining, by the processing circuitry of the other device, whether to store or discard the transmitted cardiovascular pressure based on determining whether the posture was the target posture.

An eye implant has a body including (a) a receiver, (b) a first mounting clip and (c) a second mounting clip. The receiver is adapted to hold an intraocular device to be implanted in an eye. The receiver, the first mounting clip and the second mounting clip generally extend along a common arc.

An implantable system comprising a first device, also called a centralisation device, suitable for being implanted in a fixation position inside the patient's body and at least one second device suitable for stimulating an organ of the patient when the second device is implanted, in a stimulation position, in the patient's body. The first device being further configured to command a stimulation of the organ by the second device. The implantable system being characterised in that the organ is a separate organ from the stomach and in that, when the first device is in the fixation position, the first device is accommodated in the patient's stomach and fixed to a stomach wall.

A sensing device may include a housing and one or more features configured to couple the housing against the outer surface of the bone of the patient. A sensing device may include onboard electronics carried by the housing, the onboard electronics comprising: communication circuitry, one or more sensors configured to generate data regarding one or more characteristics of the patient; and processing circuitry configured to activate the communication circuitry to send the generated data to a device outside the patient.

A stretch-measurement probe includes an elongate outer sleeve, expansion feature associated with a distal portion of the outer sleeve, and an elongate inner rod disposed at least partially within the outer sleeve. The expansion feature is configured to allow a longitudinal distance between a proximal end of the outer sleeve and the distal end of the outer sleeve to be varied.

Described herein are flexible and stretchable LED arrays and methods utilizing flexible and stretchable LED arrays. Assembly of flexible LED arrays alongside flexible plasmonic crystals is useful for construction of fluid monitors, permitting sensitive detection of fluid refractive index and composition. Co-integration of flexible LED arrays with flexible photodetector arrays is useful for construction of flexible proximity sensors. Application of stretchable LED arrays onto flexible threads as light emitting sutures provides novel means for performing radiation therapy on wounds.

A medical electrode array system comprising a thin-film substrate, a plurality of electrode contacts disposed on the thin-film substrate, and a plurality of traces. The plurality of electrode contacts is configured to provide electrical contact points. The plurality of traces is electrically connected to the plurality of electrode contacts. A electrode contact of the plurality of electrode contacts has a dedicated trace of the plurality of traces that provides electrical connectivity to the electrode contact. The thin-film substrate is configured to flex to maintain continuous contact with contours of patient anatomy. The plurality of traces includes flexible spring-like portions to add flexibility to the thin-film substrate.

A sensor implantation assembly is disclosed that includes a tissue puncture closure device. The tissue puncture closure device has a proximal end portion and a distal end portion and a suture extending from the proximal end portion to the distal end portion. A suture anchor assembly is also included that is insertable through a tissue wall puncture. The suture anchor assembly is attached to the suture at the distal end portion of the closure device and has a diagnostic sensor. A sealing pad is positioned around the suture at the distal end portion and is slidable along the suture. The diagnostic sensor may be placed within a tissue wall to gather diagnostic information such as pressure measurements at or near the site of the tissue puncture closure.