Abstract: Methods for treating cutaneous conditions and dermatoses such as disorders of the skin, subcutaneous tissues, mucous membranes, poorly vascularized tissues and/or other tissue disorders, including erosions, fissures, transient and/or chronic sores, burns, wounds, ulcers, lesions and infections. In particular embodiments, treatments include methods for improving skin and related tissue healing and repair using oxygen microbubbles (OMBs) and/or various formulations and/or compounds incorporating OMBs in combination with various other medicaments and/or tissue implants.

Abstract: Disclosed are improved devices, systems and methods for storing, protecting and/or dispensing/delivering products that are particularly sensitive to pressure changes, alterations in gas distributions and/or partial pressures, physical impacts, temperature changes and/or other variations in the ambient environment.

Abstract: Disclosed are improved devices, systems, methods and compositions containing therapeutic lipid monolayer stabilized gas microfoam(s) that can be applied to the skin after a treatment which “damages” or otherwise modifies one or more skin layers, which can improve a patient's recovery time, reduce swelling, scarification and/or callous formation, reduce skin sensitivity and/or lead to a more desirable appearance in a shorter period of time than existing skin treatments.

Abstract: Disclosed are improved devices, systems and methods for storing, protecting and/or dispensing/delivering products that are particularly sensitive to pressure changes, alterations in gas distributions and/or partial pressures, physical impacts, temperature changes and/or other variations in the ambient environment.

Abstract: The invention relates to an improved oxygen microbubble (OMB)-and-Cannabidiol (CBD) formulation that can be administered for medical and/or therapeutic purposes in any entry route and delivery method to improve bioavailability and half-life within the body. The dual CBD-OMB emulsion/formulation described herein may be a product capable of simultaneously delivering oxygen and CBD to a target tissue of interest to also further enhance blood flow to the target tissue site potentially increasing the uptake of CBD by the anatomy and thereby enhancing CBD's bioavailability in humans.

Abstract: Disclosed are improved devices, systems and methods of delivering oxygen and/or other therapeutic substances to a living organism, such as a mammal and/or human patient, by delivering and/or circulating microbubble carriers within existing anatomical passages of the organism that are accessible via external body orifices, such as portions of the organism's digestive and/or excretory tracts.

Abstract: Disclosed are improved devices, systems and methods of delivering oxygen and/or other therapeutic substances into and/or through the skin of a living organism, such as a mammal and/or human patient, by applying compounds incorporating microbubble carriers to the external surface of the individual's skin.

Abstract: Methods for treating cutaneous conditions and dermatoses such as disorders of the skin, subcutaneous tissues, mucous membranes, poorly vascularized tissues and/or other tissue disorders, including erosions, fissures, transient and/or chronic sores, burns, wounds, ulcers, lesions and infections. In particular embodiments, treatments include methods for improving skin and related tissue healing and repair using oxygen microbubbles (OMBs) and/or various formulations and/or compounds incorporating OMBs in combination with various other medicaments and/or tissue implants.

Abstract: An apparatus comprises a body portion having a sidewall with one or more threads and defining a lumen. The apparatus includes a brace portion having a sidewall that defines a lumen that is fluidically coupled to the lumen of the body portion. The sidewall of the brace portion has one or more threads that are configured to matingly couple to the threads of the body portion. The brace portion has a contact surface configured to contact a bodily tissue of a patient when a cannula is disposed within the lumen of the body portion and the lumen of the brace portion. The brace portion and the body portion are collectively configured to maintain a position of the cannula within a body of the patient relative to the bodily tissue when the cannula is disposed within the lumen of the brace portion and the lumen of the body portion.

Abstract: A spinal implant device for fusing adjacent vertebra having a first base member, a second base member and a center section. The center section is designed to provide flexibility between the first base member and the second base member. A channel extends through the implant from the first base member through the center section to the second base member to allow for bone growth through the implant device.