US2017050019A1PendingUtilityA1

Esthetic device for beautifying skin and methods thereof

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Assignee: VENUS CONCEPT LTDPriority: Sep 5, 2011Filed: Nov 3, 2016Published: Feb 23, 2017
Est. expirySep 5, 2031(~5.1 yrs left)· nominal 20-yr term from priority
A61B 2018/1467A61N 1/328A61N 1/06A61B 2018/00452A61N 1/0476A61F 7/007A61B 18/18A61B 2018/0047A61B 18/203A61N 7/02A61N 2007/0034A61B 2018/00791A61B 2018/00005A61N 5/0616A61N 5/0625A61F 2007/0052A61B 18/14A61N 1/403
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Claims

Abstract

A device for improving the cosmetic appearance of the skin is disclosed, wherein said device comprises RF generating means for generating N independent RF signals of predetermined waveforms, frequencies, amplitudes, and relative phases; control means for controlling the output of said RF generating means, said control means in communication with said RF generating means; N pairs of RF electrodes, each of said pairs in independent communication with said RF generating means, said RF electrodes configured to transmit RF energy to said skin; and an electrically insulating casing adapted to hold said RF electrodes such that said RF electrodes may be placed in simultaneous physical contact with said skin.

Claims

exact text as granted — not AI-modified
1 . A device for improving the cosmetic appearance of the skin, comprising:
 a. an RF generator that is configured to generate N independent RF signals of predetermined waveforms, frequencies, amplitudes, and relative phases;   b. N pairs of RF electrodes, each of said N pairs of electrodes characterized by a proximal end and a distal end, each of said pairs in independent communication with said RF generator, said RF electrodes configured to transmit RF energy to said skin;   c. a controller that is configured to control the output of said RF generator, said controller in communication with said RF generator; and,   d. an electrically insulating casing configured to hold said N pairs of RF electrodes at said proximal end such that said N pairs of RF electrodes may be placed in simultaneous physical contact with said skin;   wherein said N independent RF signals are phase shifted relative to one another;   further wherein said distal ends of said electrodes are in a substantially horizontal configuration.   
     
     
         2 . The device according to  claim 1 , wherein at least one of the following is being held true:
 a. the time-dependent amplitude A t,m  of the mth of said N independent RF signals is given by the relationship A t,m =A 0,m ·F m (ω m t+φ m ), where A 0,m  is a predetermined constant which is greater than or equal to 1, F m  is a predetermined periodic function of time, ω m  is the angular frequency of the mth RF signal, and φ m is a predetermined phase shift of the mth RF signal; for each of said N independent RF signals, φ m =πk(j−1)/N, where 0≦k≦1, m=1, 2, 3 . . . N and j is an integer equal to or greater than 1; where N is the amount of said RF electrode pairs; Fm is chosen from a group consisting of sine, cosine, tan, cotangents (cot), sawtooth wave, triangular wave, square wave, rectangular wave, trapezoidal wave, and any combination of the above;   b. each of said predetermined frequencies is between about 1 Hz and about 100 MHz.   c. said RF signals are transmitted in either a continuous mode or in pulses; when the RF is applied in pulses, the length of said pulses is between about 0.01 micro-sec and about 1 ms; length of said pulses is between about 0.1 and about 1000 ms;   d. additionally comprising a mechanism configured to apply Pulsed Electromagnetic Field Therapy (PEMF);   e. further comprising at least one temperature sensor configured to measure the temperature of the surface of said skin; said at least one sensor chosen from a group consisting of impedance meter configured to measure impedance across at least one of said N pairs of RF electrodes; thermal sensor; thermometer; and any combination thereof; said at least one temperature sensor is configured to either come into contact with the skin or not be in contact with the skin; said controller is programmed to regulate the amount of RF energy transmitted to said skin such that the temperature of said skin remains within a predetermined range; said predetermined range is between ambient temperature and 42° C.;   f. said N pairs of RF electrodes are disposed about the distal end of said casing in a geometry chosen from a group consisting of linear; zigzag; on the perimeter of a shape chosen from substantially polygonal, circular, oval, or irregular; within the area of a shape chosen from polygonal, circular, oval, or irregular; and any combination of the above;   g. the power transmitted by said RF electrodes and said RF generator to said skin is between 1 W and 700 W;   h. said cosmetic improvement is chosen from a group consisting of skin rejuvenation, reduction of the number of wrinkles, reduction of the depth of wrinkles, reduction of cellulite, skin tightening, circumferential reduction, and any combination of the above;   i. further comprising cooling means configured to cool said skin;   j. said cooling means are chosen from a group consisting of a Peltier effect cooling device, irrigation with cool water, and means for blowing air across the skin;   k. said N pairs of RF electrodes are further configured to provide heat to said skin;   l. additionally comprising a skin massaging section; and,   m. at least one of said N pairs of RF electrodes comprises a hypodermic syringe for penetrating into subcutaneous tissue.   
     
     
         3 . The device according to  claim 1 , further comprising a deep tissue diathermy device. 
     
     
         4 . The device according to  claim 3 , wherein at least one of the following is being held true:
 a. said deep tissue diathermy device is chosen from a group consisting of: a device emitting RF radiation and any other means configured for producing electrical current absorbed by subcutaneous tissue;   b. said deep tissue diathermy device further comprises at least one electrical output device configured to generate RF electromagnetic energy; and, at least two electrodes electrically coupled to said electrical output device and placed on said skin region, wherein all said electrodes are configured to simultaneously apply said RF electromagnetic energy to said skin;.   c. said deep tissue diathermy device further comprises at least one electrical output device configured to generate electrical current; and, at least two electrodes electrically coupled to said electrical output device and placed on said skin region, wherein all of said electrodes are configured to simultaneously apply said electrical current to said skin;.   d. said deep tissue diathermy device is chosen from a group consisting of: an acoustic diathermy device, an optical diathermy device, an electromagnetic induction diathermy device, a device for producing sound waves, an ultrasonic diathermy device, and a device for direct application of heat;   e. said deep tissue diathermy device is an optical device configured to emit light in wavelengths absorbed by subcutaneous tissue such that said subcutaneous tissue is heated;   f. said deep tissue diathermy device is a device configured to emit sound waves of a frequency absorbed by the subcutaneous tissue such that said subcutaneous tissue is heated;   g. said controller is configured to monitor physical tissue parameters and to change at least one of a group consisting of: (a) the amount of heat applied and (b) the form of said RF in response to the values of said physical tissue parameters; and,   h. said controller further comprises:   a processor that is configured to direct the storage, in a communicable database, of predetermined parameters defining safe and unsafe treatment parameters, said parameters chosen from a group consisting of time of said treatment, temperature of said skin, frequency, power, energy applied by said RF generator, depth to which said device operates, magnetic field intensity, tissue impedance, specific absorption rate, superficial muscle contractions and any combination thereof;   a sensor that is configured to sense electromagnetic radiation and heat radiation parameters chosen from a group consisting of time of said treatment, temperature of said tissue, frequency, power, intensity of ultrasound irradiation, energy applied by said RF generator, depth to which said device operates, magnetic field intensity, tissue impedance, specific absorption rate, superficial muscle contractions and any combination thereof; and,   a regulator that is configured to stop the operation of said device if said parameters are determined to be unsafe.   
     
     
         5 . The device according to  claim 1 , wherein said controller is configured to change said N independent RF signals according to predetermined medical needs, and comprising:
 a. at least one sensor that is configured to monitor electrotherapy parameters related to the level of skin rejuvenation and viability;   b. a processor that is configured to determine the degree of esthetic improvement in at least one tissue parameter related to the level of skin rejuvenation and vitality; and,   c. a regulator that is configured to stop the operation of said device when said degree of esthetic improvement reaches a predetermined value.   
     
     
         6 . The device according to  claim 5 , wherein at least one of the following is being held true:
 a. said electrotherapy parameters are chosen from a group consisting of dermal tensile forces, tissue impedance, muscle contraction forces, skin elasticity, and any combination thereof;   b. said at least one tissue parameter is chosen from a group consisting of dermal tensile forces, tissue impedance, muscle contraction forces, skin elasticity, and any combination thereof;   c. said at least one sensor that is configured to monitor electrotherapy parameters is chosen from a group consisting of time of said treatment, temperature of said tissue, frequency, power, tissue impedance, superficial muscle contractions and any combination thereof; and,   d. said processor is configured to direct the storage, in a communicable database, of predetermined parameters defining safe and unsafe treatment conditions; said predetermined parameters are chosen from a group consisting of time of said safe and unsafe treatment, temperature of said tissue, frequency, power, tissue impedance, superficial muscle contractions, and any combination thereof.

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