Abstract: A therapeutic garment includes at least one first expandable bladder configured to underlie a wearer's left shoulder blade, at least one second expandable bladder configured to underlie the wearer's right shoulder blade, and an actuator configured to alternatingly (a) expand the at least one first expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a rightward direction and (b) expand the at least one second expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a leftward direction.

Abstract: A method for implanting a breast implant into a subject, the method includes: providing a sterile, flexible, elastic biodegradable bag sized to contain the breast implant; providing a sterile breast implant; inserting, using sterile handling, the sterile breast implant into the sterile bag to form a sterile breast implant assembly; closing the bag to fully enclose the implant within the bag; and implanting in a sterile manner the sterile breast implant assembly into the subject. A sterile bag, which may be provided in a kit, preferably for use with the method includes first and second chambers connected by a channel for moving a breast implant from the first chamber through the channel to the second chamber without directly touching the implant. An incision dilator may also be included with the kit or separately provided for use in a preferred embodiment of the method.

Abstract: A therapeutic garment includes at least one first expandable bladder configured to underlie a wearer's left shoulder blade, at least one second expandable bladder configured to underlie the wearer's right shoulder blade, and an actuator configured to alternatingly (a) expand the at least one first expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a rightward direction and (b) expand the at least one second expandable bladder from a collapsed state to an expanded state such that the wearer's torso is rolled in a leftward direction.

Abstract: A biodegradable cover or coating for a breast implant includes a biodegradable cover or coating over the breast implant and contains one or more drugs for delivery at the surgical site, particularly for treating or preventing infection, pain, inflammation, capsular contracture, scarring or other indication or complication associated with breast augmentation or breast reconstruction.

Abstract: A method for implanting a breast implant into a subject, the method includes: providing a sterile, flexible, elastic biodegradable bag sized to contain the breast implant; providing a sterile breast implant; inserting, using sterile handling, the sterile breast implant into the sterile bag to form a sterile breast implant assembly; closing the bag to fully enclose the implant within the bag; and implanting in a sterile manner the sterile breast implant assembly into the subject. A sterile bag, which may be provided in a kit, preferably for use with the method includes first and second chambers connected by a channel for moving a breast implant from the first chamber through the channel to the second chamber without directly touching the implant. An incision dilator may also be included with the kit or separately provided for use in a preferred embodiment of the method.

Abstract: A device and method for alleviating pressure on a portion of a patient's body that may be bed-ridden or otherwise constrained for long periods of time. A position of the mechanism is based upon a location or distribution of angiosomes in the body portion. The mechanism includes a pump, and a portable garment with inflatable channels and pressure relievers. The channels provide varying pressure on the body portion, a maximum pressure being set at a level sufficient for treating or preventing decubitus ulcer formation on the body portion. The channels are positioned based upon angiosome distribution in the portion of the body. The pressure relievers protect tissue on bony prominences from excess pressure.

Abstract: An apparatus for treating or preventing decubitus ulcers includes: a garment sized and shaped to be worn by a patient; a first plurality of fluid channels and a second plurality of fluid channels coupled to the garment and disposed adjacent to one another, at least some of the first plurality of fluid channels being independently inflatable and deflatable as compared with at least some of the second plurality of fluid channels; and a fluid control mechanism coupled to the first and second plurality of fluid channels and operating to repeatably and sequentially inflate and deflate the independently inflatable and deflatable fluid channels from among the first and second plurality of fluid channels such that there is less than a predetermined level of pressure exerted on the patient's tissue under one or more of the deflated channels.

Abstract: System and methods for collecting and preparing fat for autologous fat tissue transplantation. The system includes syringes, filtering and transferring assemblies coupled with the syringes, a centrifuge and a centrifuge insert releasably coupled with the centrifuge. Substances, including oil, fat, and denser substances, such as tumescent fluid, connective tissue, hormones and/or other non-fat substances, are harvested through a cannula into a syringe. Syringes are placed in the centrifuge insert, and subject to centrifugation. Centrifugation stratifies the substances into a top oil stratum, a middle fat stratum, and a bottom denser substance stratum. Denser substances are filtered out of the syringes during or after centrifugation. Oil is removed through an aspiration port in the plunger head of the syringe plunger. Fat is transferred from the first syringe into one or more smaller syringes through an adapter in the assembly coupled with the first syringe and the smaller syringe.

Abstract: System and methods for collecting and preparing fat for autologous fat transplantation. The system includes a centrifuge, syringes, and filtering and transferring assemblies coupled with the syringes. Substances, including oil, fat, and denser substances (tumescent fluid, connective tissue, and other non-fat substances), are harvested into a syringe. A dye is provided or injected in the syringe. Centrifugation of the syringe stratifies the substances into a top oil stratum, a middle fat stratum, and a bottom denser substance stratum. A superficial layer of less viable fat tissue in the middle stratum is highlighted by the dye. Denser substances are filtered out of the syringes during centrifugation. Oil and the less viable fat tissue are removed through a port in the plunger head of the syringe plunger. More viable fat tissue is transferred into smaller syringes through an adapter in the assembly coupled with the syringe and the smaller syringes.

Abstract: System and methods for collecting and preparing fat for autologous fat transplantation. The system includes a centrifuge, syringes, and filtering and transferring assemblies coupled with the syringes. Substances, including oil, fat, and denser substances (tumescent fluid, connective tissue, and other non-fat substances), are harvested into a syringe. A dye is provided or injected in the syringe. Centrifugation of the syringe stratifies the substances into a top oil stratum, a middle fat stratum, and a bottom denser substance stratum. A superficial layer of less viable fat tissue in the middle stratum is highlighted by the dye. Denser substances are filtered out of the syringes during centrifugation. Oil and the less viable fat tissue are removed through a port in the plunger head of the syringe plunger. More viable fat tissue is transferred into smaller syringes through an adapter in the assembly coupled with the syringe and the smaller syringes.