US2022126113A1PendingUtilityA1

Portable rechargeable led red light cavity healing devices

Assignee: MARINE BIOLOGY AND ENVIRONMENTAL TECH LLCPriority: May 19, 2016Filed: Jan 7, 2022Published: Apr 28, 2022
Est. expiryMay 19, 2036(~9.8 yrs left)· nominal 20-yr term from priority
A61N 2005/0662A61N 2005/0611A61N 2005/0651A61N 2005/0626A61N 2005/0607A61N 2005/0632A61N 2005/0645A61N 2005/0606A61N 2005/063A61N 2005/0605A61N 2005/0608A61N 2005/0659A61N 5/0603A61N 5/0613
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Claims

Abstract

A light-emitting diode (LED) therapy device and method of use is provided that increases healing of tissues by targeting damaged tissue at a predetermined wavelength and pulsed at a predetermined frequency. The device includes a housing and a light radiation module enclosed within the housing. The light radiation module includes an LED, a controller unit connected to the LED to control wavelength and pulsed frequency of the LED, and a rechargeable power source. The device also includes a light-diffusing member connected to the housing designed to diffuse light emitted from the LED to damaged tissue in a human cavity. Light in the red or near infrared range and pulsed at a Nogier frequency increases the effectiveness of the LED device to stimulate healing of damaged tissues. Particular devices include incorporation into a pacifier for healing an infant's gums, or nasal, auditory, vaginal, or anal cavities and adults or children.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A light-emitting diode (LED) therapy device to target surfaces within a cavity, the device comprising:
 (i) a housing;   (ii) a light radiation module substantially enclosed within the housing, the light radiation module having,
 (a) an LED for emitting light having at least one predetermined wavelength, 
 (b) a controller unit connected to the LED, the controller unit capable of controlling pulse frequency of the LED for at least one predetermined frequency; 
 (c) a power source electrically connected to the controller unit; 
   (iii) a light diffusing member connected to the housing, the light diffusing member designed to diffuse and project light emitted from the LED.   
     
     
         2 . The device of  claim 1 , and wherein the predetermined wavelength is between 600 nm and 700 nm, and wherein the at least one predetermined frequency is at least one of a Nogier frequency and a harmonic of the Nogier frequency,
 whereby light pulsed at the Nogier frequency or the harmonic of the Nogier frequency increases the rate of tissue repair compared to the rate of tissue repair when tissue is treated by light not pulsed at the Nogier frequency.   
     
     
         3 . The device of  claim 1 ,
 wherein the predetermined wavelength is between 600 nm and 980 nm, and wherein the at least one predetermined frequency is a predetermined frequency within 30 percent of a Nogier frequency.   
     
     
         4 . The device of  claim 1 ,
 wherein the light diffusing member is a flexible silicone nipple having an outer surface, an internal cavity defined by an internal surface, a top region, a middle region, and a base region substantially encircling the LED, wherein the top region of the silicone nipple permits light from the LED to emit from the LED through the internal cavity of the nipple to the top region of the silicone nipple to exit from the top region of the silicone nipple, thereby allowing light form the LED to illuminate an oral cavity of a person when the silicone nipple is placed within the oral cavity;   wherein the power source is a rechargeable battery.   
     
     
         5 . The device of  claim 1 ,
 wherein the light radiation module further comprises a Bluetooth module and a wireless charging receiving inductive coil.   
     
     
         6 . The device of  claim 1 , further comprising:
 a mouth shield between the light radiation module and light diffusing member to prevents an infant from inserting the entirety the device into a mouth;   a light pipe positioned on top of the LED and within an internal cavity of the light diffusing member, the light pipe having a base and a top, the top of the light pipe angled to emit light at a wider angle compared to light emitted by the LED without the light pipe, thereby increasing exposure of LED light to an infant's gums;   wherein the light pipe comprises an aperture allowing for air to pass from the cavity of the nipple to a waterproof compartment enclosed by the housing, the aperture used for balancing the air pressure between the internal cavity of the light diffusing member and the waterproof compartment; and,   at least one temperature sensor embedded within or adjacent to the light diffusing member, the at least one temperature sensor adapted to measure a temperature of an infant's gums.   
     
     
         7 . The device of  claim 2 , wherein the Nogier frequency is at least one of 292 Hz, 584 Hz, and 1168 Hz. 
     
     
         8 . The device of  claim 4 , wherein the Nogier frequency is at least one of 292 Hz, 584 Hz, and 1168 Hz. 
     
     
         9 . The device of  claim 1 , wherein the housing comprises an optical guide for directing light through the housing, the housing characterized as having an elongated tubular region, the elongated tubular region having a first end in proximity to the LED and a second end opposing the first end;
 wherein the light-diffusing member is flexible silicone cap designed to attach to the second end of the elongated tubular region.   
     
     
         10 . The device of  claim 9 , wherein the removable flexible silicone cap is made from a porous and acoustically permeable material and designed to fit firmly within an ear canal of a human. 
     
     
         11 . A light-emitting diode (LED) therapy device comprising a first device of  claim 7  and a second device of  claim 7 ,
 wherein the first and the second devices are connected to each other via a bridge member; and, 
 wherein the optical guide of the first device and the optical guide of the second device are spaced between 1 and 3 centimeters from each other and designed to fit within two nostrils of a human, 
 whereby light emanating from the first and second devices is directed to a nasal cavity of a human. 
 
     
     
         12 . The device of  claim 1 , characterized as having an elongated body,
 wherein the housing is an elongated housing comprised of a transparent or translucent silicone rubber;   wherein the housing encloses an optical guide for placement of a plurality of the LEDs along a longitudinal axis of the device;   wherein the optical guide is connected to a compartment enclosing the power source; and,   wherein the power source is a rechargeable power source.   
     
     
         13 . The device of  claim 12 , further comprising an elastomeric tubular sheath designed to fit over the elongated housing and conform to the general shape of the elongated housing. 
     
     
         14 . The device of  claim 13 , wherein the elastomeric tubular sheath is coated with a lubricant to aid in insertion of the device into a cavity. 
     
     
         15 . The device of  claim 13 , wherein the elongated tubular sheath is a latex sheath. 
     
     
         16 . The device of  claim 13 , wherein the housing is characterized has having a base region, the base region having an indentation to secure the tubular sheath to the elongated housing. 
     
     
         17 . A method of promoting healing of tissues using red LEDs, comprising:
 inserting a device into an animal cavity, wherein the device includes a housing, a light radiation module substantially enclosed within the housing, an LED having at least one predetermined wavelength, a controller unit connected to the LED, the controller unit capable of controlling pulse frequency of the LED at least one predetermined frequency, a power source, and a light diffusing member connected to the housing;   illuminating the LED at a wavelength between 600 nm and 700 nm;   pulsing the LED at a Nogier frequency.   
     
     
         18 . The method of  claim 17  where in the Nogier frequency is at least one of 292 Hz, 584 Hz, and 1168 Hz. 
     
     
         19 . The method of  claim 17 , wherein inserting the device is characterized as inserting the device into at least one of a mouth, an ear canal, a nostril, an anal cavity and a vaginal cavity.

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