Abstract: The device intended for the stimulation of the brain by laser circularly or elliptically polarized light consists of the main unit (1) equipped in the front part with control buttons (3), and a display (2) from which at least one laser diode (16, 17, 18, 19) is supplied. At least one nasal applicator (8, 9, 10, 11) or nasal applicators (38, 39) suitably equipped in the rear part with laser diodes (40, 41) can be connected to the upper part of the main unit (1). The main unit (1) is supplied in its lower part through a connector (33), and the programmable control unit (51) with built-in battery (56) and autonomous processor (57) is an integral part of the device.

Abstract: A hand held device generates a predetermined number of pulses of electromagnetic radiation having a predetermined electromagnetic spectrum, a predetermined duration, a predetermined inter-pulse interval, and a predetermined total energy. The pulse sequence is delivered to a skin surface to reduce or eliminate Xray or ultraviolet radiation damage to the skin surface.

Abstract: Apparatus and method for making and using devices that generate optical signals, and optionally also electrical signals in combination with one or more such optical signals, to stimulate (i.e., trigger) and/or simulate a sensory-nerve signal in nerve and/or brain tissue of a living animal (e.g., a human), for example to treat nerve damage in the peripheral nervous system (PNS) or the central nervous system (CNS) and provide sensations to stimulate and/or simulate “sensory” signals in nerves and/or brain tissue of a living animal (e.g., a human) to treat other sensory deficiencies (e.g., touch, feel, balance, visual, taste, or olfactory) and provide sensations related to those sensory deficiencies, and/or to stimulate (i.e., trigger) and/or simulate a motor-nerve signal in nerve and/or brain tissue of a living animal (e.g., a human), for example to control a muscle or a robotic prosthesis.

Abstract: A therapeutic device includes a garment configured to be worn on a user's body over a treatment area. The therapeutic device includes a plurality of therapeutic electromagnetic (EM) energy emitting devices, fixed to the garment at locations within the garment for irradiating the treatment area with EM energy when the garment is worn over the treatment area. A power supply is fixed to and within the garment. The power supply stores electrical charge and outputs electrical supply current from the stored electrical charge. A flexible graphite material is located within the garment and conducts the electrical supply current to the EM energy emitting devices to activate the energy emitting devices.

Abstract: A microprocessor controlled medical laser device that has a precise laser beam alignment system indicated by a series of sequentially color changing LEDS. The power management system adjusts the LED'S power input so as maximize battery life, increasing it by up to six times. It's alignment is enabled by a triaxial accelerometer that may be accurately calibrated horizontally or to a plethora of angles relative to the horizontal axis. It is shock resistant and times out to turn the laser off after a predetermined time.

Abstract: Apparatus and methods for treating psychiatric disorders, mood disorders and circadian rhythm disorders with a multi-stage light protocol are disclosed. The presently disclosed multi-stage light protocol provides a synergistic treatment including up to 4 types of therapies: bright light therapy, extended sleep deprivation therapy, dawn simulation therapy and short to medium wavelength light therapy. According to some embodiments, the first stage of the protocol includes a first time window of 20 minutes during which, for a majority of the time, the light intensity is between 50 lux and 2000 lux. According to some embodiments, the second stage of the protocol includes a second time window of at least 90 minutes during which, for every 10 minute period within the second time window, for a majority of the time, the light intensity is exceeds 100 lux.

Abstract: A headgear lasing system, including: a power supply; a laser device coupled in power receiving relationship to the power supply, and configured for generating laser radiation effective to promote growth of head hair; a multiplicity of optical fibers coupled with the laser device to receive the laser radiation for transmission thereof through the optical fibers to respective end portions thereof; and a support that is configured to overlie a head region, and to which the end portions of the optical fibers are secured so that the laser radiation transmitted through the optical fibers is directed therefrom to the head region. The support may be a separate structural component that is secured to an existing headgear article, or the support may be a constituent part of a headgear article, such as a crown portion of a cap or hat article. The headgear lasing system is usefully employed to impinge lasing radiation on a scalp region of a wearer, to mediate hair growth on such scalp region.

Abstract: An output assembly is sized for placement in the middle and inner ear, such that removal of bone can be decreased. The output assembly may comprise at least one photo detector, a demultiplexer and an optical array sized to pass through an incision in the eardrum. An input transducer assembly is configured to transmit a multiplexed optical signal to the output assembly. The input assembly can be configured to transmit the multiplexed optical signal through the eardrum, such that tissue removal can be decreased and the device can be placed without removal of bone, for example. The multiplexed optical signal may comprise a pulse width modulated signal so as to decrease the effect of non-linearities of the light source and light detector and provide quality sound to the user.

Abstract: The present invention provides methods of using electromagnetic radiation in the visible portion of the spectrum to modulate mitochondrial function in the treatment of various conditions, including Alzheimer's disease, other dementias, hypoxia and diabetic peripheral neuropathy, and sensory disorders of the extremities.

Abstract: An apparatus for treatment of fungal infections and/or other foot skin disorders, comprises a shoe-type housing having a substantially hollow interior forming a treatment chamber, a supporting platform disposed within the hollow chamber; so that a foot of a patient positioned within the treatment chamber is supported by the platform, so that nails are disposed at the lower level of the front part of the chamber, whereas the heel of the foot is being elevated a rear part thereof. A delivery and control assembly for the aqueous solution is provided. At least one light delivery arrangement is disposed within or in the vicinity of the treatment chamber.

Abstract: Method and apparatus for optically stimulating neurons of a plurality of auditory nerve pathways of a person to provide auditory sensations for the person by generating a plurality of pulsed light signals having one or more successive pulses. The spectrum of a detected audio signal is divided into M channels. In some embodiments, an N-of-M coding strategy is employed, where, for any given time frame, only N of the M channels are selected and illuminated to stimulate the auditory nerves. In some embodiments, the M channels are organized into bins, where, for any given time frame, only a maximum number of channels are illuminated per bin. This limits the number of illuminated channels-per-length of cochlea and therefore prevents localized heating of the cochlea and reduces power consumption of the device.

Abstract: A method to enable a laser to interact with a structure behind a barrier includes calculating a set of characteristics for a first laser channel to be effective to tunnel through the barrier and calculating a second set of characteristics for a second laser channel to be effective to interact with the structure, generating said first laser pulse to form a tunnel through the barrier and prior to closing of the tunnel, generating the second laser pulse to travel through the tunnel to interact with the structure. A treatment unit associated with this method has a control panel in communication with an electronics package. Data entered into the control panel enables the electronics package to calculate the first and second sets of characteristics and drive a first laser generating a laser pulse of the first laser channel followed after a delay by a laser pulse of the second laser channel.

Abstract: Method and apparatus for optically and electrically stimulating neurons of auditory nerve pathways of a person to provide auditory sensations for the person including generating a plurality of pulsed light signals having one or more successive pulses, delivering the plurality of pulsed light signals to one or more auditory nerve pathways of the cochlea of the person and selectively controlling the plurality of light signals to optically stimulate and trigger nerve action potentials (NAPs) in the one or more auditory nerve pathways. In some embodiments, the present invention also includes one or more electrical stimulation electrodes used to stimulate the low frequency portions of the auditory nerves.

Abstract: A laser therapy device includes a solid-state laser configured for a CW operation and including a pump source, and a controller configured to generate at least one first pulse of the laser in a first-pulse operation. The controller is configured to switch on the pump source to a pump power level S1 at least once during the first-pulse operation. A rise time E, after which the pump power level S1 of the pump source is attainable and starting from the time the pump source is switched on, is in a range of 50 ns to 350 ns.

Abstract: A portable, small-footprint laser device contains one or more housings in which a laser energy source and an optical arrangement are disposed. The housing produces a laser beam spot that may be rotated and scanned to apply laser energy to a target area. The laser device receives treatment parameters and uses them to program a treatment regimen in which activation and movement of the housings is automated. The laser device may be used to apply a treatment regimen to a patient's hands or feet that are infected by Onychomycosis. In the treatment regimen, certain wavelengths of laser energy are applied at a predetermined duration. The treatment may be repeated, and a topical anti-fungal medication may be applied to aid in the efficacy of the treatment.

Abstract: A noninvasive method of slimming a patient's body by applying laser energy having a wavelength shorter than 632 nm externally through the skin of the patient. One or more areas of a patient's body, preferably the more fatty regions, such as the abdominal, buttock, lower back, thigh, bust or arm regions, is measured. Objective measurements are made of body criteria, including external dimension, percentage body fat, fat mass, or body mass. Sufficient laser energy, preferably in a range of 0.03-0.1 J/cm2, is applied to one or more of those areas to cause a reduction in the measurement in the lasered areas, as well as overall body slimming. The preferred embodiments use laser light at about 532 nm, 440 nm, or 405 nm. Preferably 18 mW or 25 mW laser diodes are used to apply laser energy at 0.03-0.1 J/cm2 for 15 minutes, every other day for 1-4 weeks, depending on the amount of slimming desired.

Abstract: Methods and systems for modifying tissue use a pressurized fluid stream carrying coherent light energy. The methods and systems may be used for resecting and debulking soft and hard biological tissues. The coherent light is focused within a stream of fluid to deliver energy to the tissue to be treated.

Abstract: Process and device for directly medicinally treating interior tissue during or after intubation of a patient by passing medicinal radiant energy transversely through the intubation device to irradiate the internal patient tissue for promoting healing or for an antimicrobial effect. The invention is useful in conjunction with endoscopies and catherizations, such as urinary catherization, gastric and pulmonary endoscopies, and the like procedures. The process and device can also provide liquid flow and/or vision.

Abstract: The invention relates to a device for measuring an optical penetration that is triggered in a tissue underneath the tissue surface by means of therapeutic laser radiation which a laser-surgical device concentrates in a treatment focus located in said tissue. The inventive device is provided with a detection beam path comprising a lens system which couples radiation emanating from the tissue underneath the tissue surface into the detection beam path. A detector device generating a detection signal which indicates the spatial dimension and/or position of the optical penetration in the issue is arranged downstream of the detection beam path.

Abstract: An implantable stimulation device is described which includes a flexible carrier member for implantation adjacent to target neural tissue. Carrier wires are embedded within the carrier member for conducting electrical signals. At least one active interface device also is within the carrier member and includes a hermetically sealed device housing without penetration by any electrical conductor, an active interface element within the device housing, an inductive link arrangement providing an electrical connection between the active interface element and a terminal end of one of the carrier wires, and an outer interface surface adjacent to the target neural tissue that provides a communication link between the adjacent target neural tissue and the active interface element.

Abstract: Methods and arrangements for distinguishing between target areas and non-target areas during a laser surgical procedure involve coating or otherwise providing the non-target areas with a phosphorescent material that emits radiation, upon stimulation when a predetermined condition occurs, that is distinguishable from the treatment radiation.

Abstract: A battery-powered laser-based dermatological treatment device may include a laser unit comprising at least one laser diode, a battery unit, at least one sensor configured to generate sensor signals, and a laser drive control system including a laser drive circuit comprising the laser unit, the battery unit, a first switch (e.g., a first FET), and a second switch (e.g., a second FET), wherein the laser unit is arranged in series between the first switch and the second switch, and control electronics configured to control the first switch based at least on sensor signals from the at least one sensor, and control the second switch using pulse width modulation (PWM), thereby delivering current from the battery unit to the laser unit with a PWM current waveform. The laser drive circuit may also include a snubber circuit configured to prevent voltage spikes upon the second switch being turned off.

Abstract: A laser therapy device, including: a laser diode that is adapted to produce a monochromatic laser beam; a lens that is adapted to receive the beam directly from the laser diode and exploit the natural divergence of the laser diode to form an essentially coherent monochromatic, collimated beam; wherein the formed beam is adapted to form on a plane perpendicular to the direction of propagation of the beam an elongated illuminated area in which the length of the illuminated area is at least twice the size of the width of the illuminated area; a controller that is adapted to control activation of the laser diode; an encasement enclosing the laser diode, the lens and the controller; wherein the encasement is adapted to be hand held by the user.

Abstract: A method of light therapy includes non-invasive, intra-cranial administration of bright light via the ear canal of a subject by using a light intensity of 0.7-12 lumens, and a treatment time of 1-15 minutes. A medical device including radiation elements for directing the light via the ear canal for use in the light therapy is described.

Abstract: Apparatus and method for optical- or optical-and-electrical stimulation of e.g., auditory nerve pathways, for example spiral ganglion in the cochlea or neurons in the cochlear nerve. Several configurations for guiding and directing the optical stimulation are disclosed. Several configurations for guiding and directing the electrical field (used in some embodiments, for sensitization) in and through the destination tissue to which the optical stimulation is directed are disclosed. In some embodiments, and array of IR VCSELs emit stimulation light, in particular to tissue in the cochlea for restoring hearing. In some embodiments, an electrical signal is also applied in a manner that reduces the amount of light in a pulse that is otherwise needed to elicit a NAP. In some embodiments, a heat dissipater is used to spread the heat generated by operation of the lasers and their circuits, to avoid heat damage to the tissue.

Abstract: The current invention discloses a treatment device having a heat source, a power source, a heat applicator and a lighting mechanism. The power source includes at least one nanotech battery, ensuring superior properties such as prolonged electricity production and prompt recharging. The heat applicator includes a heat conductive layer made from nanofibers, providing highly efficient heat distribution to the targeted regions. The lighting mechanism employs light emitting nano fibers to treat targeted regions. The power source provides energy to the light source, which generates light so that the applicator may distribute to an injury site or wound bed of a user. The heat source may be an exothermic chemical reaction designed to last for several hours supplying heat to the treatment device or a electronically produced heat. In addition to the medical utilizations, the current device may also play a central role in other apparatus that require thermal control or lighting capabilities.

Abstract: A non-surgical, drug-free hyperhidrosis treatment includes applying infra-red laser irradiation having a wavelength of at least approximately 1064 nm to a plurality of discrete spots in the affected area. The operating parameters of the infra-red laser are adjusted so that the irradiation penetrates the skin at each spot and deactivates the underlying sweat glands. The degree of sweat suppression is controlled by adjusting the number of and spacing between the spots. The laser light can be generated by a NdYAG laser. The spot size can be approximately 2 mm, the pulse duration approximately 0.65 ms, and the laser power approximately 9300 Watts. A prior art laser source can be used to manually implement the invention, or a special purpose apparatus can automatically deflect the infra-red beam under digital control between the desired spot locations. In embodiments, the controller further controls the laser timing and other operating parameters.

Abstract: The current invention discloses a treatment device having a heat source, a power source, a heat applicator and a lighting mechanism. The power source includes at least one battery having superior properties such as prolonged electricity production and prompt recharging. The heat applicator includes a heat conductive layer made from nanofibers, providing highly efficient heat distribution to the targeted regions. The lighting mechanism employs light emitting nano fibers to treat targeted regions. The power source provides energy to the light source, which generates light so that the applicator may distribute to an injury site or wound bed of a user. The heat source may be an exothermic chemical reaction designed to last for several hours supplying heat to the treatment device or an electronically produced heat. The treatment device further comprises a plurality of electrodes for electrical stimulation treatment.

Abstract: Methods and apparatus are provided for thermally-induced renal neuromodulation. Thermally-induced renal neuromodulation may be achieved via direct and/or via indirect application of thermal energy to heat or cool neural fibers that contribute to renal function, or of vascular structures that feed or perfuse the neural fibers. In some embodiments, parameters of the neural fibers, of non-target tissue, or of the thermal energy delivery element, may be monitored via one or more sensors for controlling the thermally-induced neuromodulation. In some embodiments, protective elements may be provided to reduce a degree of thermal damage induced in the non-target tissues.

Abstract: Method of producing a therapeutic laser device (TLD). The TLD includes stretchable, flexible membranes which comprise a high pressure air cavity. High air pressure is produced by fans which are speed controllable by computer. Standoff posts provide, an attachment function, and a separation function between the TLD and the patient. Semiconductor laser diodes and lens sets in a two dimensional array produce the therapeutic laser light. Cooling air tubes direct air controlled by temperature sensors from the high pressure cavity onto laser diodes. Capacitive proximity sensors in conjunction with infrared radiation sensors confirm close contact with a patient and allow lasing. Power is supplied either by battery or by connection to mains power. A touch screen computerized device with wireless communication displays information to the user and controls the therapy session. The TLD and the power supply both have stretchable straps enabling the TLD to be fixed to the patient.

Abstract: A hand-held self-contained nerve-stimulation device and method using light to provide a source of precise stimulation on one or more nerve fibers. In some embodiments, this simulation is provided through a device and method wherein a laser- or LED-light source is mounted to the handpiece. Light is passed from the light source through optical tip to simulate nerves. In some embodiments, the device is constructed from non-magnetic material such as glass, plastic or ceramics. In some embodiments, the light emanating from the optical tip can be controlled manually or automatically. In some embodiments, the handpiece contains a self-contained power source, such as batteries. In some embodiments, the handpiece is at least in part, activated by remote control in order to prevent moving the handpiece during activation. Some embodiments include a unit operable to sense a response of nerve stimulation and to suppress a laser-ablation surgery operation.

Abstract: A laser package for use in a dermatological treatment device may include a conductive carrier, an insulation layer arranged over a first region of a first side of the conductive carrier, a semiconductor laser device mounted to a second region of the first side of the conductive carrier, and a conductive film secured to the semiconductor laser device and extending over at least a portion of the insulation layer, such that the conductive film is insulated from the conductive carrier by the insulation layer, and wherein a coefficient of thermal expansion of the semiconductor laser device differs from a coefficient of the conductive carrier to which it is mounted by more than 20%.

Abstract: The present disclosure relates, in some embodiments, to apparatus, systems, methods, and compositions for purifying cells (e.g., adipocytes, stem cells) from mammalian tissues (e.g., adipose tissues). For example, the present disclosure relates to apparatus, systems, methods, and compositions for purifying and/or preserving adipocytes and/or stem cells from fat tissue of a mammalian subject according to some embodiments.

Abstract: Disclosed is a skin treatment device for personal use. The device includes an optical radiation providing module operating in pulsed or continuous operation mode, a mechanism for continuously displacing the device across the skin, and a device displacement speed monitoring arrangement. When the device is applied to skin, the optical pulses repetition rate establishes the power of the optical radiation as a function of the device displacement speed. The device a hair removal mechanism configured to mechanically remove hair from the treated segment of the skin.

Abstract: A method of reducing scar formation associated with a skin wound includes providing an electromagnetic energy source, delivering energy from the electromagnetic energy source to opposing edges of a skin wound, and sealing the wound after delivering the energy. The electromagnetic energy source can include a laser, such as a fractional laser, including a fractional CO2 laser. Handpieces configured to reduce scar formation include one or more of a tissue eversion system, a medication delivery system, and a wound sealing system.

Abstract: Methods and devices of treating fungal nail infections are disclosed. A portable device for treating fungal nail infections includes an irradiator configured to irradiate light of at least first and second types, and an attaching element configured to attach the radiator to a digit having a nail which is infected by a fungal infection, and to position the irradiator at a position suitable to irradiate at least part of the nail.

Abstract: Phototherapy systems comprising a therapeutic lamp platform for radiant lamps such as LEDs disposed in an assembly comprising a first wall to which the lamps are affixed thereto and a second wall, closer to the patient, spaced from the first wall wherein the lamps are recessed relative thereto. The second wall comprises a reflective surface facing towards a patient and a plurality of light apertures substantially aligned with the LEDs on the first wall for communicating lamp radiation from the lamps to a user. The lamps and associated circuitry are disposed between the first and second wall so that the reflective surface is relatively smooth and seamless towards the patient. The walls have a malleable rigidity for flexible adjustability relative to the user. The device is mounted to the user with a frame comprising an eyeglass frame or goggles including lenses for shielding the user's eyes from lamp radiation.

Abstract: A lipolysis system configured for contacting and providing low-power laser irradiation to a plurality of targeted portions of a subject's body surface for the purpose of liquefying fats in subcutaneous regions underlying the targeted body surface portions, and methods for the use of the lipolysis system. The lipolysis system comprises: (a) a first laser applicator comprising a plurality of low-power laser diodes selected for emission of power outputs in the range comprising about 10 mW to about 100 mW with light waves in the range of 635 nm to 680 nm, (b) a second laser applicator comprising at least one low-power laser diode selected for emission of power outputs in the range comprising about 10 mW to about 100 mW with light waves in the range of 635 nm to 680 nm, and (c)a laser control device configured for controllably communicating and cooperating with said first laser applicator and said second laser applicator.

Abstract: An improved procedure for performing liposuction is obtained by utilizing a needle that includes a laser source conductor with one end of the needle being configured for insertion into a target adipose skin volume and the other end being coupled to a laser source. The needle may include one or more channels for extracting the treated adipose area. A vacuum source can be used in the extraction of the treated adipose. Further, the first end of the needle may include a cap or end-piece that reduces the build up of carbon deposits. A temperature sensor may be used as input to adjust the laser power and prevent over exposure.

Abstract: Techniques disclosed herein include systems and methods for treating spinal cord injury. Techniques include using a diode laser assembly, a power source, a fiber optic cable, and a fenestrated tip. The power source can be connected to the diode laser assembly, with a fiber optic cable connected to the diode laser assembly. The fenestrated tip is connected to the fiber optic cable to emit a plurality of laser light beams produced by the diode laser assembly at a location remote from the diode laser assembly. The apparatus can be used in a method for treating a spinal cord injury. The method is carried out by providing a source of laser light having a wavelength in the range of 500-1000 nm and a power in the range of 5 to 500 milliwatts. The laser light is transmitted through an optical wire to a position adjacent a spinal cord injury site, with at least a portion of the apparatus positioned within a human body. The spinal cord injury site is then irradiated with laser light from the optical wire.

Abstract: Provided is a handpiece of a laser treatment device which can restrict a temperature rise of body tissues in a path from an irradiation portion to a target region more effectively than in the related art. The handpiece 10 includes an optical fiber 16 which guides laser light emitted from a pulse light source, and a revolving holder which holds a tip portion 64 of the optical fiber 16 such that the tip portion 64 is tilted with respect to a rotational axis C0 to direct an optical axis C1 of the laser light towards a target point P located on the rotational axis C0 and revolves the tip portion 64 of the optical fiber 16 about the rotational axis C0. Further, a pulse number of the pulse light source per unit time and a number of revolutions of the tip portion 64 of the optical fiber 16 per unit time are determined such that the pulse number of the pulse light source per unit time is not an integral multiple of the number of rotations of the tip portion 64 of the optical fiber 16 per unit time.

Abstract: In general, in one aspect, the disclosure features a system that includes a flexible waveguide having a hollow core extending along a waveguide axis and a region surrounding the core, the region being configured to guide radiation from the CO2 laser along the waveguide axis from an input end to an output end of the waveguide. The system also includes a handpiece attached to the waveguide, wherein the handpiece allows an operator to control the orientation of the output end to direct the radiation to a target location of a patient and the handpiece includes a tip extending past the output end that provides a minimum standoff distance between the output end and the target location.

Abstract: Method and apparatus in which optical sources deliver light to small specific areas of the cochlea for purposes of stimulation, which brings the advantage of increased spectral fidelity because the stimulation illumination can be more specifically placed than electrical-stimulation signals. In some embodiments, a plurality of light sources or light delivery devices are placed at finely-spaced locations along the cochlea but only a fraction of them are used within any short period of time due to the limitation of power delivery to the optical emitters and a restriction on heat within the cochlea due to the absorption of the optical stimulation signals. The ability to choose which optical sources are used at any given time frame provides the ability to choose the sources that illuminate and thus stimulate the particular small areas of the cochlea that generate nerve signals perceived as the semitone frequencies found in Western music.

Abstract: A hair restoration caring device includes a treatment hood, a suspension member and a hair caring device. The treatment hood is to be disposed over a user's head. The suspension member is fastened to the treatment hood. The hair caring device is attached to the suspension member and is movable with respect to the user scalp. The hair caring device includes an outer casing mounted slidably on the suspension member, and has several downward combing projections and several light emitters installed above the combing projections respectively for radiating light waves. Each combing projection is aligned with a respective light emitter and is formed with an axial passage to permit past through of light waves of the respective light emitter.

Abstract: Method of producing a therapeutic laser device (TLD). The TLD includes stretchable, flexible membranes which comprise a high pressure air cavity. High air pressure is produced by fans which are speed controllable by computer. Standoff posts provide, an attachment function, and a separation function between the TLD and the patient. Semiconductor laser diodes and lens sets in a two dimensional array produce the therapeutic laser light. Cooling air tubes direct air controlled by temperature sensors from the high pressure cavity onto laser diodes. Capacitive proximity sensors in conjunction with infrared radiation sensors confirm close contact with a patient and allow lasing. Power is supplied either by battery or by connection to mains power. A touch screen computerized device with wireless communication displays information to the user and controls the therapy session. The TLD and the power supply both have stretchable straps enabling the TLD to be fixed to the patient.

Abstract: The device for interstitial laser thermotherapy of tumors comprises an hollow needle (3) with a point (3A) for perforating a tissue (T) to be treated, and a light guide (9) which can be inserted in said hollow needle. The hollow needle is associated with a membrane (17) which is inflatable to form a balloon (P) into which the distal end (9A) of said light guide (9) can project, the membrane being inflated to create a cavity in the tissue to be treated into which laser radiation is guided by said light guide.

Abstract: A platform Smart Scalpel system using rapid real-time feedback for effecting laser treatment. The platform system includes an imaging system for rapid real-time detection of tissue characteristics, a processing system for processing the detected characteristics, and a treatment system for effecting treatment in accordance with results of the processing. The platform system provides for preprogramming and real-time inputting conditions and parameters for diagnosis using the imaging system and/or treatment using the treatment system.

Abstract: A non-surgical method for improving both the external pubic appearance and the internal vaginal tightness of a female patient in a single procedure includes providing a cosmetic skin-tightening device having a wand having a tip that applies heating energy to skin collagen, where the wand is shaped such that the tip can be inserted into the patient's vagina. During the procedure, the wand is alternately passed over the external pubic skin and inserted into the patient's vagina, thereby tightening both the pubic and vaginal regions during a single procedure while preventing overheating of any one area. The heat energy can be conductively transmitted heat or a radiated energy such as infra-red, laser, or radio frequency energy. A disposable sleeve can be applied over the wand to facilitate cleaning and sterilization after use. A vaginal lubricant and/or ultrasound gel can be applied.

Abstract: Apparatuses for treatment of hyperhidrosis, Raynaud's phenomenon, cerebral ischemia and asthma and hypertension by nerve stimulation are disclosed. In particular, the invention relates to the improvement of these conditions by stimulating at least one ganglion selected from the group consisting of T-1 through T-4 ganglia, cervical ganglia, renal nerve or combinations thereof with an implantable, wireless, battery-less and lead-less stimulator. Stimulations of the ganglion may be carried out with pulsed radiofrequency, thermal energy or optical irradiation.

Abstract: Aspects for treating spinal cord injuries are disclosed. In a particular aspect, a method includes identifying a neurological level of a spinal cord injury, and activating neurons via laser therapy in which a laser beam is applied to an area proximate to the neurological level. In another aspect, a computer-readable storage medium includes computer-readable instructions for performing various acts. Such acts comprise ascertaining a neurological level of a spinal cord injury, and receiving data corresponding to a severity of the spinal cord injury. The acts further comprise outputting a laser calibration according to the neurological level and the severity. A medical device apparatus is also provided, which includes various computer executable components. The computer executable components include an assessment component configured to receive parameters corresponding to a spinal cord injury, and a calibration component configured to ascertain a laser calibration according to the at least one parameter.